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| Sponsor: | Children's Hospital of Eastern Ontario |
|---|---|
| Collaborators: |
US Congress Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Canadian Institutes of Health Research (CIHR) Juvenile Diabetes Research Foundation European Foundation for the Study of Diabetes European Community (EC) Mead Johnson Nutrition Finnish Diabetes Research Foundation Academy of Finland Dutch Diabetes Research Foundation |
| Information provided by: | Children's Hospital of Eastern Ontario |
| ClinicalTrials.gov Identifier: | NCT00179777 |
Purpose
The Trial to Reduce IDDM in the Genetically at Risk (TRIGR) is an international effort to conduct a primary prevention nutrition trial for type 1 (insulin-dependent) diabetes. The TRIGR study is targeted at newborns who are at genetic risk for type 1 diabetes because their mother, father and/or full sibling has type 1 diabetes. All families are encouraged to breast feed their infants for as long as possible. Prior to birth, the child is randomly assigned to receive one of two infant formulas, should formula be required prior to 8 months of age. The study will determine whether weaning to a possibly protective infant formula decreases these children's chances of developing diabetes - as it does in the animal models for diabetes.
| Condition | Intervention | Phase |
|---|---|---|
|
Diabetes Mellitus, Type 1 |
Dietary Supplement: hydrolysed vs nonhydrolysed infant formula vs breast feeding |
Phase II |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | TRIGR - Trial to Reduce IDDM in the Genetically at Risk |
| Enrollment: | 2032 |
| Study Start Date: | March 2002 |
| Estimated Study Completion Date: | February 2017 |
| Estimated Primary Completion Date: | February 2017 (Final data collection date for primary outcome measure) |
The hypothesis for this study is that weaning to an extensively hydrolyzed infant formula will decrease the incidence of type 1 diabetes in subjects with risk-associated HLA genotypes and a first degree relative with type 1 diabetes, as it does in all relevant animal models for the disease.
Specific Aims:
I.a: To determine if weaning to a case in hydrolysate infant formula reduces the frequency of diabetes-predictive auto-antibodies in subjects with risk-associated HLA genotype and a first degree relative with type 1 diabetes (mother, father and/or full sibling).
I-b: To determine if weaning to a casein hydrolysate infant formula reduces the frequency of clinical diabetes in subjects with risk-associated HLA genotype and an affected first degree relative.
A secondary aim is to determine relationships between cow's milk antibodies, a measure of cow's milk exposure, and diabetes-associated auto-antibodies.
The mother of the unborn child is recruited during pregnancy. Randomization to one of two infant formulas takes place before birth (after 35 weeks gestation) or immediately after birth.
Experimental Arm: Use of extensively hydrolysed cow's milk based infant formula when needed in supplementation or substitution for breast milk through 6-8 months from birth.
Control Arm: Use of non-hydrolysed cow's milk based infant formula when needed in supplementation or substitution for breast milk through 6-8 months from birth.
All families are encouraged to breast feed their infants for as long as possible. The study infant formula is only used if exclusive breast feeding ceases before 8 months of age.
Cord blood for genotyping is obtained at birth, or failing that from a heel prick by 7 days of age. Only subjects with genotypes indicating increased genetic risk for type 1 diabetes remain in the intervention trial. All other subjects are withdrawn from the study.
All subjects will be followed for 10 years.
Eligibility| Ages Eligible for Study: | up to 7 Days |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Pennsylvania | |
| University of Pittsburgh | |
| Pittsburgh, Pennsylvania, United States, 15213-2583 | |
| Australia, New South Wales | |
| Children's Hospital at Westmead | |
| Westmead, New South Wales, Australia, 2145 | |
| Canada | |
| Robarts Research Institute | |
| London, Canada, N6A 5K8 | |
| Czech Republic | |
| 3rd Faculty of Medicine, Charles University, University Hospital Vinohrady | |
| Prague, Czech Republic, 10 | |
| Estonia | |
| Tartu University Children's Hospital | |
| Tartu, Estonia, 51014 | |
| Finland | |
| University of Helsinki | |
| Helsinki, Finland, 00029HUS | |
| Germany | |
| Kinderkrankenhaus auf der Bult | |
| Hannover, Germany, 30173 | |
| Hungary | |
| Semmelweis Medical University | |
| Budapest, Hungary, 1083 | |
| Italy | |
| St. Michele Hospital | |
| Cagliari, Sardinia, Italy, 09134 | |
| University Campus Bio-Medico of Rome | |
| Rome, Italy, 00155 | |
| Luxembourg | |
| Centre Hospitalier de Luxembourg | |
| Luxembourg, Luxembourg, 1210 | |
| Netherlands | |
| Sophia Children's Hospital | |
| Rotterdam, Netherlands, 3015 GJ | |
| Poland | |
| Medical University of Wroclaw | |
| Wroclaw, Poland, 50-376 | |
| Spain | |
| Hospital de Cruces | |
| Barakaldo, Vizcaya, Spain, 48903 | |
| Hospital Clinico San Carlos | |
| Madrid, Spain, 28040 | |
| Sweden | |
| University of Linkoping | |
| Linkoping, Sweden, S-58185 | |
| Switzerland | |
| University Children's Hospital | |
| Zurich, Switzerland, CH-8032 | |
| Principal Investigator: | Hans K Akerblom, MD | Helsinki University |
More Information
| Responsible Party: | Principal Investigator: Hans K Akerblom, MD, University of Helsinki, Helskinki, Finland |
| ClinicalTrials.gov Identifier: | NCT00179777 History of Changes |
| Other Study ID Numbers: | MCT-49395, U01 HD40364, U01 HD42444 |
| Study First Received: | September 10, 2005 |
| Last Updated: | February 7, 2008 |
| Health Authority: | Finland: Ethics Committee |
|
Diabetes Mellitus, Type 1 Genetic Predisposition to Disease Infant Nutrition Primary Prevention |
|
Diabetes Mellitus Diabetes Mellitus, Type 1 Glucose Metabolism Disorders Metabolic Diseases |
Endocrine System Diseases Autoimmune Diseases Immune System Diseases |