It's easier than you think to help find ways to cure, prevent and treat type 1 diabetes.

Researchers all over Australia are running clinical trials for type 1 diabetes. If you would like to participate or learn more about one of these trials, use our clinical trial finder below. 

These are the current clinical trials in your state. If none of these are suited to you at this point, sign up to become a T1D Game Changer, and we'll keep you updated as to when new trial opportunities arise. 

Researchers: Submit your clinical research project on our trial finder.

Australian Capital Territory | New South Wales | Northern Territory | Queensland | South Australia | Tasmania | Victoria | Western Australia

 Photo: The Salmon family of New South Wales. Max (age 6) was diagnosed with type 1 diabetes in 2010.

Trial Finder:

Australian Capital Territory

TrialNet: Pathway to Prevention Study to Prevent Type 1 Diabetes (T1D) 

Family members of people with T1D are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research institute (Seattle, USA) and recruiting from Canberra Hospital Paediatric Research.

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • Individuals aged 2.5-45 with an immediate family member with T1D
  • Individuals aged 2.5-20 with an extended family member with T1D
  • have not been diagnosed with diabetes 

This study is listed on the Clinical Trials Registry: NCT00097292.

For more information about the study contact the study coordinator here.

Updated 10th September 2019.

New South Wales

Nox 1/4 Inhibition to Treat Kidney Disease in Type 1 Diabetes (T1D)

This study will test whether a new tablet can help to treat diabetic kidney disease. The study will last for 56 weeks, and participants will be allocated to receive either the new tablet or placebo. There will be 10 study visits. The study led by the Baker Heart and Diabetes Institute (Prof Jonathan Shaw) and recruiting patients from Royal North Shore Hospital and Hunter Diabetes Centre in NSW.

The study, funded by the T1DCRN, is currently recruiting adults (18-70 years) with T1D, with HbA1c<10%, and with albumin (protein) in the urine.

The study has been approved by the South Metropolitan Health Service Human Research Ethics Committee (HREC) and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12617001187336.

For more information about the study contact the study coordinator at:

Email

For more information click here.

The Fenofibrate and Microvascular Events in Type 1 DiabetIc Retinopathy (FAME-1-EYE) Study

The FAME-1-Eye Study is investigating whether fenofibrate, a drug that is already on the market to lower cholesterol and blood fats, can slow or reverse eye damage and other complications in adults with T1D. We know that fenofibrate improves blood fats and slows the progression of eye damage in people with type 2 diabetes, this study will see if it has the same effect in T1D. The study led by the Clinical Trials Centre, University of Sydney (Prof Alicia Jenkins) and recruiting patients from multiple sites in NSW.

The study, funded by JDRF, the T1DCRN and the National Health and Medical Research Council (NHMRC) is currenting recruiting adults with T1D and non-proliferative retinopathy.

The study has been approved by the Northern Sydney Local Health District Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12611000249954.

For more information about the study contact the study coordinator at NHMRC Clinical Trials Centre.

Email: fame1eye@ctc.usyd.edu.au

Phone: 1800 158 629

For more information click here

Environmental Determinants of Islet Autoimmunity (ENDIA)

The ENDIA study is looking into what contributes to the development of T1D in early childhood. T1D in children is twice as common as it was 20 years ago. This is because our environment has changed and predisposed children are more likely to develop T1D. If we can understand exactly what in the environment is harmful or protective, we can develop strategies to prevent T1D.

The study led by the Royal Adelaide Hospital (Prof Jennifer Couper) and recruiting patients from Children’s Hospital at Westmead, Royal Hospital for Women and St George Hospital, NSW.

The study, funded by JDRF, the T1DCRN and Helmsley Charitable Trust is currenting recruiting:

  • Women who are pregnant with a baby that will have a first-degree relative with T1D
  • A man with T1D whose partner is pregnant
  • A child with T1D whose mum is pregnant

The study has been approved by the Women's and Children's Health Network Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register: ACTRN12613000794707.

For more information about the study contact the study coordinator at Royal Adelaide Hospital:

Email: endia@adelaide.edu.au 

Phone: (08) 8161 8747

For more information click here

Investigation of a Closed Loop Device for Young People with T1D

A hybrid closed loop system  provides automated control of basal insulin delivery, offering the potential to reduce glucose variability outside of the healthy  range compared with standard treatment. This study will explore the use of a hybrid closed loop system (Medtronic Minimed 670G) vs. standard treatment (current pump or multiple daily injections with or without continuous glucose monitoring) on health outcomes and quality of life. The study led by the Princess Margaret Hospital for Children (Prof Timothy Jones) and recruiting patients from The Children’s hospital Westmead and the John Hunter Children’s hospital in NSW.

The study, funded by the T1DCRN/JDRF, is currenting recruiting children with aged 12-25 years with T1D (duration >1 year) treated with either multiple daily injections or an insulin pump and with HbA1c <10.5%.

The study has been approved by the Princess Margaret Hospital Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12616000753459

For more information about the study contact the study coordinator at the Perth Children’s Hospital

Email: diabetes.research@health.wa.gov.au

For more information click here.

ToGeTher: Type One Diabetes and Gut Therapy 

Recent research has shown that a specialised fibre supplement can prevent T1D in mice by influencing the gut microbiome (e.g. gut bacteria). This study is the first to trial this fibre supplement in adults already diagnosed with T1D to see whether there are any changes to your overall health, diabetes management and your gut microbiota. Participants will need to consume the fibre for 6 weeks and attend 5 appointments over 12 weeks. 

Inclusion criteria:  Adults (18-45 years) with T1D (>6 months duration) and stable management (not still producing your own insulin or not changed recently between injections and a pump), HbA1c <8.5%, no history or symptoms of gastrointestinal disease or malabsorption (e.g. coeliac disease), weight between 50-120kg, no antibotic usage currently or during the study.  

The study has been approved by the SLHD RPAH Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12618001391268

For more information about the study contact the study coordinator at Charles Perkins Centre, University of Sydney:

Dr Kirstine Bell

Email: kirstine.bell@sydney.edu.au 

Phone: + 61 400 167 043

Find out more.

The Australasian Diabetes Data Network (ADDN)

ADDN connects real-time diabetes data about thousands of type 1 diabetes patients from specialist centres across on a single platform that allows for a long-term monitoring of diabetes outcomes and participation in clinical research.

The study co-led by the Australasian Paediatric Endocrine Group (APEG) and the Australia Data Society (ADS) is recruiting patients from the Children's Hospital at Westmead (Sydney, NSW) and the John Hunter Children's Hospital (Newcastle, NSW)

The study, funded by the JDRF and the T1DCRN, is currenting recruiting children and adults with T1D.

The study has been approved by the Hunter New England Human Research Ethics Committee.

For more information about the study contact the ADDN study coordinator:

Email: info@addn.org.au 

For more information click here.

Pathway to Prevention Study to prevent Type 1 Diabetes

Family members of people with type 1 diabetes are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research Institute (Seattle, USA) and recruiting patients from Hunter Diabetes Centre, John Hunter Hospital, Royal North Shore Hospital and Westmead Children’s hospital, NSW.  

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • are between the ages of 2.5 and 45 years and have a parent, brother/sister, or child with T1D
  • are between the ages of 2.5 and 20 years and have an aunt/uncle, cousin, grandparent, niece/nephew, or half-brother/sister with T1D
  • have not been diagnosed with diabetes

The study is listed on the clinicaltrials.gov registry: NCT00097292

For more information about the study contact the study coordinator here.

How does the type of dietary protein influence postprandial glycaemia in type 1 diabetes?

The iBolus:Protein Study will research the impact of the type of dietary protein on postprandial (after meal) blood glucose levels in adults with type 1 diabetes using an insulin pump. The study will compare 5 different types of protein (egg, beef, chicken, salmon and whey protein isolate) each served with 45g of carbohydrate (rice). The study involves 5 sessions, for 5.5 hours per session, total commitment 27.5 hours. 

Inclusion criteria: Aged 18-70 years with type 1 diabetes (>1 year duration), insulin pump therapy for greater than or equal to 3 months, HbA1c less than or equal to 8.5%, reliably performing self-monitoring of blood glucose levels at least four times daily/or using continuous glucose monitoring, fluency in English.

The study has been approved by the SLHD RPAH Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12618001344280

For more information about the study contact the study coordinator at Charles Perkins Centre, University of Sydney:

Dr Kirstine Bell

Email: kirstine.bell@sydney.edu.au 

Phone: + 61 400 167 043

Find out more

Cord Reinfusion in Diabetes (CORD) Pilot Study

Cell Care is partnering with The Children’s Hospital at Westmead, New South Wales, in a world–first study investigating the potential of cord blood to prevent or delay the onset of type 1 diabetes (T1D) in children at high risk of developing the disease.

The CORD study is currently recruiting children between 1 and 14 years of age who are at high risk of developing T1D – where a parent, sibling or other close family members (1st or 2nd degree relatives) have T1D. The study is available to families who have stored cord blood or who are currently expecting a baby and planning cord blood storage.

If you have a family history of Type 1 diabetes and are expecting a child, you can request your cord blood and tissue information pack here.

For more information about the CORD study contact the CORD Study coordinator/nurse at The Children's Hospital Westmead;
Email: SCHN-CHW-CORD@health.nsw.gov.au
Phone: (02) 9845 3512

The CORD study has been approved by the Sydney Children's Hospitals Network Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trial Register: ACTRN12613000186752

Is dysfunction of brain blood vessels associated with cognitive impairment in type 1 diabetes? (INeuroT1D) 

The study group's goal is to estimate the contributions of age and diabetes-specific brain changes observed in older age T1D. Namely, they aim to evaluate cerebral blood vessel function and blood flow as well as hearing control and their relationships with how well the brain performs during mental tasks, and if type 1 diabetes can impact this performance in later life, when compared to non-diabetic participants.

Inclusion criteria: Age 30-80 years, T1D diagnosed before 18 years, No advanced T1D complications such as blindness or deafness, Not hospitalised for severe glycemic events in the last 3 months, No liver or kidney disease, No malignant cancer, Not pregnant, No neurological conditions including stroke, TIA, major depression, multiple sclerosis, parkinson's disease, dementia or mild cognitive impairment. 

The INeuroT1D study is listed on the Australian and New Zealand Clinical Trial Register: ACTRN12618000496213

For more information about the INeuroT1D study contact the Study coordinator at University of Newcastle NSW.

Email: rachel.wong@newcastle.edu.au
Phone: (02) 4921 6408

INTIMET: INsulin Resistance in Type 1 Diabetes Managed with METformin

This is a detailed study of liver and muscle insulin resistance in adults with type 1 diabetes. The investigators will study the efficacy of adjunctive metformin in reversing insulin resistance and improve glucometabolic status, endothelial health and other parameters. Predictors of response to metformin will be assessed.

The study is led by the Garvan Institute of Medical Research/Prof Jerry R Greenfield and is recruiting patients from Westmead Hospital and St Vincent’s Hospital. The study is currenting recruiting adults (20-50) with T1D (at least 10 years since diagnosis and have a HbA1c ≤ 9.5%.

The study has been approved by the St. Vincent’s Hospital HREC and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12619001440112

For more information about the study contact Dr Jennifer Snaith at Garvan:

Email: INTIMET@garvan.org.au 

Phone: 0491731769

Updated 10th September 2019

Northern Territory

Pathway to Prevention Study to prevent Type 1 Diabetes

Family members of people with type 1 diabetes are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research Institute (Seattle, USA) has multiple sites around Australia recruiting patients.

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • are between the ages of 2.5 and 45 years and have a parent, brother/sister, or child with T1D
  • are between the ages of 2.5 and 20 years and have an aunt/uncle, cousin, grandparent, niece/nephew, or half-brother/sister with T1D
  • have not been diagnosed with diabetes

The study is listed on the clinicaltrials.gov registry: NCT00097292

For more information about the study contact the study coordinator here.

Updated 10th September 2019

Queensland

The Australasian Diabetes Data Network (ADDN)

ADDN connects real-time diabetes data about thousands of type 1 diabetes patients from specialist centres across on a single platform that allows for a long-term monitoring of diabetes outcomes and participation in clinical research. The study co-led by the Australasian Paediatric Endocrine Group (APEG) and the Australia Data Society (ADS) is recruiting patients from The Lady Cilento Children's Hospital, Brisbane, QLD

The study, funded by the JDRF and the T1DCRN, is currenting recruiting children and adults with T1D.

The study has been approved by the Hunter New England Human Research Ethics Committee.

For more information about the study contact the study coordinator at Royal Melbourne Hospital:

Email: info@addn.org.au 

For more information click here.

Pathway to Prevention Study to prevent Type 1 Diabetes

Family members of people with type 1 diabetes are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research Institute (Seattle, USA) has multiple sites around Australia recruiting patients.

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • are between the ages of 2.5 and 45 years and have a parent, brother/sister, or child with T1D
  • are between the ages of 2.5 and 20 years and have an aunt/uncle, cousin, grandparent, niece/nephew, or half-brother/sister with T1D
  • have not been diagnosed with diabetes

The study is listed on the clinicaltrials.gov registry: NCT00097292

For more information about the study contact the study coordinator here.

Environmental Determinants of Islet Autoimmunity (ENDIA)

The ENDIA (Environmental Determinants of Islet Autoimmunity) study is looking into what contributes to the development of Type 1 Diabetes in early childhood. Type 1 Diabetes in children is twice as common as it was 20 years ago. This is because our environment has changed and predisposed children are more likely to develop Type 1 Diabetes. If we can understand exactly what in the environment is harmful or protective, we can develop strategies to prevent Type 1 Diabetes.

The study led by the Royal Adelaide Hospital (Prof Jennifer Couper) and recruiting patients from Mater Hospital, Wesley, QLD.

The study, funded by JDRF, the T1DCRN and Helmsley Charitable Trust is currenting recruiting:

  • Women who are pregnant with a baby that will have a first-degree relative with T1D
  • A man with T1D whose partner is pregnant
  • A child with T1D whose mum is pregnant

The study has been approved by the Women's and Children's Health Network HREC and is listed on the Australian and New Zealand Clinical Trials Register : ACTRN12613000794707.

For more information about the study contact the study coordinator at Royal Adelaide Hospital:

Email: endia@adelaide.edu.au 

Phone: (08) 8161 8747

For more information click here

Updated 10th September 2019

South Australia

Nox Inhibition to Treat Kidney Disease in Type 1 Diabetes (T1D)

This study will test whether a new tablet can help to treat diabetic kidney disease. The study will last for 56 weeks, and participants will be allocated to receive either the new tablet or placebo. There will be 10 study visits. The study led by the Baker Heart and Diabetes Institute (Prof Jonathan Shaw) and recruiting patients from Royal Adelaide Hospital, SA.

The study, funded by the T1DCRN, is currenting recruiting adults (18-70years) with T1D, with HbA1c<10%, and with albumin (protein) in the urine.

The study has been approved by the South Metropolitan Health Service Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12617001187336.

For more information about the study contact the study coordinator at Royal Adelaide Hospital

Email: Health.CALHNResearchGovernance@sa.gov.au 

For more information click here.

The Fenofibrate and Microvascular Events in Type 1 DiabetIc Retinopathy (FAME-1-EYE) Study

The FAME-1-Eye Study is investigating whether fenofibrate, a drug that is already on the market to lower cholesterol and blood fats, can slow or reverse eye damage and other complications in adults with T1D. We know that fenofibrate improves blood fats and slows the progression of eye damage in people with type 2 diabetes, this study will see if it has the same effect in T1D. The study led by the Clinical Trials Centre, University of Sydney (Prof Alicia Jenkins) and recruiting patients from the Repatriation General Hospital and the Royal Adelaide Hospital.

The study, funded by JDRF, the T1DCRN and the National Health and Medical Research Council (NHMRC) is currenting recruiting adults with T1D and non-proliferative retinopathy.

The study has been approved by the Northern Sydney Local Health District Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12611000249954.

For more information about the study contact the study coordinator at NHMRC Clinical Trials Centre.

Email: fame1eye@ctc.usyd.edu.au

Phone: 1800 158 629

For more information click here

Investigation of a Closed Loop Device for Young People with T1D

A hybrid closed loop system  provides automated control of basal insulin delivery, offering the potential to reduce glucose variability outside of the healthy  range compared with standard treatment. This study will explore the use of a hybrid closed loop system (Medtronic Minimed 670G) vs. standard treatment (current pump or multiple daily injections with or without continuous glucose monitoring) on health outcomes and quality of life. The study led by the Princess Margaret Hospital for Children (Prof Timothy Jones) and recruiting patients from the  Women and Children’s Hospital Adelaide, SA.

The study, funded by the T1DCRN/JDRF, is currenting recruiting children with aged 12-25 years with T1D (duration >1 year) treated with either multiple daily injections or an insulin pump and with HbA1c <10.5%.

The study has been approved by the Princess Margaret Hospital Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12616000753459

For more information about the study contact the study coordinator at the Perth Children’s Hospital

Email: diabetes.research@health.wa.gov.au

For more information click here.

The Australasian Diabetes Data Network (ADDN)

ADDN connects real-time diabetes data about thousands of type 1 diabetes patients from specialist centres across on a single platform that allows for a long-term monitoring of diabetes outcomes and participation in clinical research.

The study co-led by the Australasian Paediatric Endocrine Group (APEG) and the Australia Data Society (ADS) is recruiting patients from the Women and Children's Hospital Adelaide and Lyell McEwin and Modbury Hospitals, Adelaide, SA.

The study, funded by the JDRF and the T1DCRN, is currenting recruiting children and adults with T1D.

The study has been approved by the Hunter New England Human Research Ethics Committee.

For more information about the study contact the ADDN study coordinator:

Email: info@addn.org.au 

For more information click here.

Pathway to Prevention Study to Prevent Type 1 Diabetes (T1D) 

Family members of people with T1D are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research institute (Seattle, USA) and recruiting from Women's and Children's Hospital, SA.

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • Individuals aged 2.5-45 with an immediate family member with T1D
  • Individuals aged 2.5-20 with an extended family member with T1D
  • have not been diagnosed with diabetes 

This study is listed on the Clinical Trials Registry: NCT00097292.

For more information about the study contact the study coordinator here.

Environmental Determinants of Islet Autoimmunity (ENDIA)

The ENDIA study is looking into what contributes to the development of T1D in early childhood. T1D in children is twice as common as it was 20 years ago. This is because our environment has changed and predisposed children are more likely to develop T1D. If we can understand exactly what in the environment is harmful or protective, we can develop strategies to prevent T1D.

The study led by the Royal Adelaide Hospital (Prof Jennifer Couper) and recruiting patients from the Women’s and Children’s Hospital, SA.

The study, funded by JDRF, the T1DCRN and Helmsley Charitable Trust is currenting recruiting:

  • Women who are pregnant with a baby that will have a first-degree relative with T1D
  • A man with T1D whose partner is pregnant
  • A child with T1D whose mum is pregnant

The study has been approved by the Women's and Children's Health Network Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register: ACTRN12613000794707.

For more information about the study contact the study coordinator at Royal Adelaide Hospital:

Email: endia@adelaide.edu.au 

Phone: (08) 8161 8747

For more information click here

Updated 10th September 2019

Tasmania

Pathway to Prevention Study to prevent Type 1 Diabetes

Family members of people with type 1 diabetes are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research Institute (Seattle, USA) has multiple sites around Australia recruiting patients.

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • are between the ages of 2.5 and 45 years and have a parent, brother/sister, or child with T1D
  • are between the ages of 2.5 and 20 years and have an aunt/uncle, cousin, grandparent, niece/nephew, or half-brother/sister with T1D
  • have not been diagnosed with diabetes

The study is listed on the clinicaltrials.gov registry: NCT00097292

For more information about the study contact the study coordinator here.

Victoria

Nox Inhibition to Treat Kidney Disease in Type 1 Diabetes (T1D)

This study will test whether a new tablet can help to treat diabetic kidney disease. The study will last for 56 weeks, and participants will be allocated to receive either the new tablet or placebo. There will be 10 study visits. The study led by the Baker Heart and Diabetes Institute (Prof Jonathan Shaw) and recruiting patients from the Baker IDI Heart and Diabetes Institute, The Alfred Hospital, Monash Health, The Austin Hospital, St Vincent’s Hospital Melbourne, Royal Melbourne Hospital, Barwon Health and Western Health.

The study, funded by the T1DCRN, is currenting recruiting adults (18-70years) with T1D, with HbA1c<10%, and with albumin (protein) in the urine.

The study has been approved by the South Metropolitan Health Service Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12617001187336.

For more information about the study contact the study coordinator at Baker Heart and Diabetes Institute:

Maria Lawton
T +61 3 8532 1835
Maria.Lawton@baker.edu.au

For more information click here.

The Fenofibrate and Microvascular Events in Type 1 DiabetIc Retinopathy (FAME-1-EYE) Study

The FAME-1-Eye Study is investigating whether fenofibrate, a drug that is already on the market to lower cholesterol and blood fats, can slow or reverse eye damage and other complications in adults with T1D. We know that fenofibrate improves blood fats and slows the progression of eye damage in people with type 2 diabetes, this study will see if it has the same effect in T1D. The study led by the Clinical Trials Centre, University of Sydney (Prof Alicia Jenkins) and recruiting patients from St Vincent’s Hospital Melbourne, Baker Heart and Diabetes Institute and University Hospital Geelong.

The study, funded by JDRF, the T1DCRN and the National Health and Medical Research Council (NHMRC) is currenting recruiting adults with T1D and non-proliferative retinopathy.

The study has been approved by the Northern Sydney Local Health District Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12611000249954.

For more information about the study contact the study coordinator at NHMRC Clinical Trials Centre.

Email: fame1eye@ctc.usyd.edu.au

Phone: 1800 158 629

For more information click here

Investigation of a Closed Loop Device for Young People with T1D

A hybrid closed loop system  provides automated control of basal insulin delivery, offering the potential to reduce glucose variability outside of the healthy  range compared with standard treatment. This study will explore the use of a hybrid closed loop system (Medtronic Minimed 670G) vs. standard treatment (current pump or multiple daily injections with or without continuous glucose monitoring) on health outcomes and quality of life. The study led by the Princess Margaret Hospital for Children (Prof Timothy Jones) and recruiting patients from the Royal Children’s Hospital Melbourne.

The study, funded by the T1DCRN/JDRF, is currenting recruiting children with aged 12-25 years with T1D (duration >1 year) treated with either multiple daily injections or an insulin pump and with HbA1c <10.5%.

The study has been approved by the Princess Margaret Hospital Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12616000753459

For more information about the study contact the study coordinator at the Perth Children’s Hospital

Email: diabetes.research@health.wa.gov.au

For more information click here.

The Australasian Diabetes Data Network (ADDN)

ADDN connects real-time diabetes data about thousands of type 1 diabetes patients from specialist centres across on a single platform that allows for a long-term monitoring of diabetes outcomes and participation in clinical research.

The study co-led by the Australasian Paediatric Endocrine Group (APEG) and the Australia Data Society (ADS) is recruiting patients from The Royal Children's Hospital, Melbourne, Monash Children's Hospital, The Royal Melbourne Hospital, St Vincent's Hospital and Sunshine Hospital, Melbourne, VIC.

The study, funded by the JDRF and the T1DCRN, is currenting recruiting children and adults with T1D.

The study has been approved by the Hunter New England Human Research Ethics Committee.

For more information about the study contact the ADDN study coordinator:

Email: info@addn.org.au 

For more information click here.

Pathway to Prevention Study to Prevent Type 1 Diabetes (T1D) 

Family members of people with T1D are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research institute (Seattle, USA) and recruiting from Baker IDI Heart and Diabetes Institute,  Monash Health and Royal Melbourne Hospital, VIC.

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • Individuals aged 2.5-45 with an immediate family member with T1D
  • Individuals aged 2.5-20 with an extended family member with T1D
  • have not been diagnosed with diabetes 

This study is listed on the Clinical Trials Registry: NCT00097292.

For more information about the study contact the study coordinator here.

Environmental Determinants of Islet Autoimmunity (ENDIA)

The ENDIA study is looking into what contributes to the development of T1D in early childhood. T1D in children is twice as common as it was 20 years ago. This is because our environment has changed and predisposed children are more likely to develop T1D. If we can understand exactly what in the environment is harmful or protective, we can develop strategies to prevent T1D.

The study led by the Royal Adelaide Hospital (Prof Jennifer Couper) and recruiting patients from Monash Health and Royal Melbourne Hospital, VIC.

The study, funded by JDRF, the T1DCRN and Helmsley Charitable Trust is currenting recruiting:

  • Women who are pregnant with a baby that will have a first-degree relative with T1D
  • A man with T1D whose partner is pregnant
  • A child with T1D whose mum is pregnant

The study has been approved by the Women's and Children's Health Network Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register: ACTRN12613000794707.

For more information about the study contact the study coordinator at Royal Adelaide Hospital:

Email: endia@adelaide.edu.au 

Phone: (08) 8161 8747

For more information click here

Hydroxychloroquine in Individuals At-risk for Type 1 Diabetes Mellitus

This study is testing a medication, called hydroxychloroquine (HCQ) to assess safety and effectiveness to prevent individuals at risk of type 1 diabetes (T1D) from progressing to type 1 diabetes.

HCQ is approved by the U.S. Food and Drug Administration as a treatment for malaria, lupus, and rheumatoid arthritis. HCQ has been used extensively for treatment of autoimmune disease in adults, children, and during pregnancy. This medication has not previously been studied as a treatment to prevent T1D.

The goal of this study is to learn if HCQ can help prevent or delay progression from normal glucose tolerance (Stage 1) to abnormal glucose tolerance (Stage 2) or type 1 diabetes (Stage 3). The study involves 5 visits in the first 6 months, then 1 visit every 6 months for the remainder of the study.

The study led by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (Carla Greenbaum, MD) is currently recruiting patients from the Walter and Eliza Hall Institute of Medical Research, VIC.

The study is listed on the clinicaltrials.gov registry here.

For more information click here.

Updated 10th September 2019 

Western Australia

Nox Inhibition to Treat Kidney Disease in Type 1 Diabetes (T1D)

This study will test whether a new tablet can help to treat diabetic kidney disease. The study will last for 56 weeks, and participants will be allocated to receive either the new tablet or placebo. There will be 10 study visits. The study led by the Baker Heart and Diabetes Institute (Prof Jonathan Shaw) and recruiting patients from Fremantle Hosptial, WA.

The study, funded by the T1DCRN, is currenting recruiting adults (18-70years) with T1D, with HbA1c<10%, and with albumin (protein) in the urine.

The study has been approved by the South Metropolitan Health Service Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12617001187336.

For more information about the study contact the study coordinator at Baker Heart and Diabetes Institute:

Maria Lawton
T +61 3 8532 1835
Maria.Lawton@baker.edu.au

For more information click here.

The Fenofibrate and Microvascular Events in Type 1 DiabetIc Retinopathy (FAME-1-EYE) Study

The FAME-1-Eye Study is investigating whether fenofibrate, a drug that is already on the market to lower cholesterol and blood fats, can slow or reverse eye damage and other complications in adults with T1D. We know that fenofibrate improves blood fats and slows the progression of eye damage in people with type 2 diabetes, this study will see if it has the same effect in T1D. The study led by the Clinical Trials Centre, University of Sydney (Prof Alicia Jenkins) and recruiting patients from Fremantle Hospital, WA.

The study, funded by JDRF, the T1DCRN and the National Health and Medical Research Council (NHMRC) is currenting recruiting adults with T1D and non-proliferative retinopathy.

The study has been approved by the Northern Sydney Local Health District Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12611000249954.

For more information about the study contact the study coordinator at NHMRC Clinical Trials Centre.

Email: fame1eye@ctc.usyd.edu.au

Phone: 1800 158 629

For more information click here

Investigation of a Closed Loop Device for Young People with T1D

A hybrid closed loop system  provides automated control of basal insulin delivery, offering the potential to reduce glucose variability outside of the healthy  range compared with standard treatment. This study will explore the use of a hybrid closed loop system (Medtronic Minimed 670G) vs. standard treatment (current pump or multiple daily injections with or without continuous glucose monitoring) on health outcomes and quality of life. The study led by the Princess Margaret Hospital for Children (Prof Timothy Jones) and recruiting patients from Princess Margaret Hospital for Children, WA. 

The study, funded by the T1DCRN/JDRF, is currenting recruiting children with aged 12-25 years with T1D (duration >1 year) treated with either multiple daily injections or an insulin pump and with HbA1c <10.5%.

The study has been approved by the Princess Margaret Hospital Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register (ANZCTR): ACTRN12616000753459

For more information about the study contact the study coordinator at the Perth Children’s Hospital

Email: diabetes.research@health.wa.gov.au

For more information click here.

The Australasian Diabetes Data Network (ADDN)

ADDN connects real-time diabetes data about thousands of type 1 diabetes patients from specialist centres across on a single platform that allows for a long-term monitoring of diabetes outcomes and participation in clinical research.

The study co-led by the Australasian Paediatric Endocrine Group (APEG) and the Australia Data Society (ADS) is recruiting patients from Perth Children's Hospitala and Fiona Stanley Hospital, Perth, WA. 

The study, funded by the JDRF and the T1DCRN, is currenting recruiting children and adults with T1D.

The study has been approved by the Hunter New England Human Research Ethics Committee.

For more information about the study contact the ADDN study coordinator:

Email: info@addn.org.au 

For more information click here.

Pathway to Prevention Study to Prevent Type 1 Diabetes (T1D) 

Family members of people with T1D are at increased risk of developing the disease. This risk can be clarified using a blood test for antibodies, which are found in around 1 in 30 family members. Those with antibodies are offered opportunities to participate in trials of therapies to prevent them ever getting diabetes. The study led by the Benaroya Research institute (Seattle, USA) and recruiting from Princess Margaret Hospital, WA.

The study, funded by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) in collaboration with JDRF, is currenting recruiting children and adults who are:

  • Individuals aged 2.5-45 with an immediate family member with T1D
  • Individuals aged 2.5-20 with an extended family member with T1D
  • have not been diagnosed with diabetes 

This study is listed on the Clinical Trials Registry: NCT00097292.

For more information about the study contact the study coordinator here.

Updated 10th September 2019 

Environmental Determinants of Islet Autoimmunity (ENDIA)

The ENDIA study is looking into what contributes to the development of T1D in early childhood. T1D in children is twice as common as it was 20 years ago. This is because our environment has changed and predisposed children are more likely to develop T1D. If we can understand exactly what in the environment is harmful or protective, we can develop strategies to prevent T1D.

The study led by the Royal Adelaide Hospital (Prof Jennifer Couper) and recruiting patients from Princess Margaret Hospital, WA.

The study, funded by JDRF, the T1DCRN and Helmsley Charitable Trust is currenting recruiting:

  • Women who are pregnant with a baby that will have a first-degree relative with T1D
  • A man with T1D whose partner is pregnant
  • A child with T1D whose mum is pregnant

The study has been approved by the Women's and Children's Health Network Human Research Ethics Committee and is listed on the Australian and New Zealand Clinical Trials Register: ACTRN12613000794707.

For more information about the study contact the study coordinator at Royal Adelaide Hospital:

Email: endia@adelaide.edu.au 

Phone: (08) 8161 8747

For more information click here

Updated 10th September 2019