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TRIGR - Primary Prevention Study for Type 1 Diabetes in Children at Risk
This study is ongoing, but not recruiting participants.
First Received: September 10, 2005   Last Updated: February 7, 2008   History of Changes
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 (EFSD)
European Community (EC)
Mead Johnson
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: Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: TRIGR - Trial to Reduce IDDM in the Genetically at Risk

Resource links provided by NLM:


Further study details as provided by Children's Hospital of Eastern Ontario:

Primary Outcome Measures:
  • Type 1 diabetes mellitus assessed by (1) blood glucose and HbA1c at 12 and 18 months of age, and annually from age 2 to 10 years, and (2) oral glucose tolerance test at 6 and 10 years of age. [ Time Frame: 12 and 18 months and annually from 2 to 10 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Diabetes associated islet antibodies (ICA, IAA, GADA, IA-2A) at 3, 6, 9, 12 and 18 months of age, and annually from age 2 to 10 years [ Time Frame: 3, 6, 9, 12, 18 months and annually from 2 to 10 years ] [ Designated as safety issue: No ]

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)
Intervention Details:
    Dietary Supplement: hydrolysed vs nonhydrolysed infant formula vs breast feeding
    hydrolysed vs nonhydrolysed infant formula vs breast feeding
Detailed Description:

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
Criteria

Inclusion Criteria:

  • Biological parent and/or full (not half) sibling of the newborn infant has type 1 diabetes as defined by the World Health Organization
  • The infant's parent or legal guardians give signed consent to participate

Exclusion Criteria:

  • An older sibling of the newborn infant has been included in the TRIGR intervention
  • Multiple gestation
  • The parents are unwilling or unable to feed the infant cow's milk based products for any reason (e.g., religious, cultural).
  • The newborn infant has a recognizable severe illness such as those due to chromosomal abnormality, congenital malformation, respiratory failure needing assisted ventilation, enzyme deficiencies, etc.
  • The gestational age of the newborn infant is less than 35 weeks.
  • The infant is older than 7 days at randomization.
  • Inability of the family to take part in the study (e.g. the family has no access to any of the Study Centers, the family has no telephone).
  • The infant has received any infant formula other than Nutramigen prior to randomization.
  • No HLA sample drawn before the age of 8 days.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00179777

  Show 17 Study Locations
Sponsors and Collaborators
Children's Hospital of Eastern Ontario
US Congress
Canadian Institutes of Health Research (CIHR)
Juvenile Diabetes Research Foundation
European Foundation for the Study of Diabetes (EFSD)
European Community (EC)
Mead Johnson
Finnish Diabetes Research Foundation
Academy of Finland
Dutch Diabetes Research Foundation
Investigators
Principal Investigator: Hans K Akerblom, MD University of Helsinki
  More Information

Additional Information:
Publications:
Responsible Party: University of Helsinki, Helskinki, Finland ( Principal Investigator: Hans K Akerblom, MD )
Study ID Numbers: MCT-49395, U01 HD40364, U01 HD42444
Study First Received: September 10, 2005
Last Updated: February 7, 2008
ClinicalTrials.gov Identifier: NCT00179777     History of Changes
Health Authority: Finland: Ethics Committee

Keywords provided by Children's Hospital of Eastern Ontario:
Diabetes Mellitus, Type 1
Genetic Predisposition to Disease
Infant Nutrition
Primary Prevention

Additional relevant MeSH terms:
Autoimmune Diseases
Metabolic Diseases
Immune System Diseases
Diabetes Mellitus, Type 1
Diabetes Mellitus
Endocrine System Diseases
Glucose Metabolism Disorders

ClinicalTrials.gov processed this record on November 30, 2009