TrialNet Pathway to Prevention of T1D

Status: Recruiting
Location: See all (22) locations...
Study Type: Observational
SUMMARY

Rationale: The accrual of data from the laboratory and from epidemiologic and prevention trials has improved the understanding of the etiology and pathogenesis of type 1 diabetes mellitus (T1DM). Genetic and immunologic factors play a key role in the development of T1DM, and characterization of the early metabolic abnormalities in T1DM is steadily increasing. However, information regarding the natural history of T1DM remains incomplete. The TrialNet Natural History Study of the Development of T1DM (Pathway to Prevention Study) has been designed to clarify this picture, and in so doing, will contribute to the development and implementation of studies aimed at prevention of and early treatment in T1DM. Purpose: TrialNet is an international network dedicated to the study, prevention, and early treatment of type 1 diabetes. TrialNet sites are located throughout the United States, Canada, Finland, United Kingdom, Italy, Germany, Sweden, Australia, and New Zealand. TrialNet is dedicated to testing new approaches to the prevention of and early intervention for type 1 diabetes. The goal of the TrialNet Natural History Study of the Development of Type 1 Diabetes is to enhance our understanding of the demographic, immunologic, and metabolic characteristics of individuals at risk for developing type 1 diabetes. The Natural History Study will screen relatives of people with type 1 diabetes to identify those at risk for developing the disease. Relatives of people with type 1 diabetes have about a 5% percent chance of being positive for the antibodies associated with diabetes. TrialNet will identify adults and children at risk for developing diabetes by testing for the presence of these antibodies in the blood. A positive antibody test is an early indication that damage to insulin-secreting cells may have begun. If this test is positive, additional testing will be offered to determine the likelihood that a person may develop diabetes. Individuals with antibodies will be offered the opportunity for further testing to determine their risk of developing diabetes over the next 5 years and to receive close monitoring for the development of diabetes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 45
Healthy Volunteers: t
View:

• Individuals 2 to 45 years old who have an immediate family member with type 1 diabetes (such as a child, parent, or sibling)

• Individuals 2-20 years old who have an extended family member with type 1 diabetes (such as a cousin, niece, nephew, aunt, uncle, grandparent, or half-sibling)

• Those aged 2 years to 45 years who are not family members and are known to have 1 or more islet antibodies

Locations
United States
California
Childrens Hospital of Orange County
RECRUITING
Orange
University of California San Francisco
RECRUITING
San Francisco
Stanford University Medical Center
RECRUITING
Stanford
Colorado
Barbara Davis Center for Childhood Diabetes
RECRUITING
Denver
Connecticut
Yale University School of Medicine
RECRUITING
New Haven
Florida
University of Florida
RECRUITING
Gainesville
Georgia
Emory Children's Center
RECRUITING
Atlanta
Indiana
Riley Hospital for Children, Indiana University
RECRUITING
Indianapolis
Massachusetts
Joslin Diabetes Center
RECRUITING
Boston
Minnesota
University of Minnesota
RECRUITING
Minneapolis
Missouri
The Children's Mercy Hospital
RECRUITING
Kansas City
New York
Columbia University
RECRUITING
New York
Pennsylvania
Children's Hospital of Pittsburgh of UPMC
RECRUITING
Pittsburgh
Tennessee
Vanderbilt University
RECRUITING
Nashville
Texas
University of Texas Medical Center at Dallas
RECRUITING
Dallas
Baylor College of Medicine
RECRUITING
Houston
Washington
Benaroya Research Institute
RECRUITING
Seattle
Other Locations
Australia
Walter and Eliza Hall Institute
RECRUITING
Parkville
Canada
The Hospital for Sick Children
RECRUITING
Toronto
Finland
University of Turku
SUSPENDED
Turku
Italy
Vita-Salute San Raffaele University
SUSPENDED
Milan
United Kingdom
University of Bristol
SUSPENDED
Bristol
Contact Information
Primary
TrialNet Central Information Center general info
1-800-425-8361
Time Frame
Start Date: 2004-02-01
Estimated Completion Date: 2030-07-31
Participants
Target number of participants: 75000
Treatments
Annual Re-Testing/Annual Metabolic Monitoring
Participants will be monitored annually for risk of type 1 diabetes.
Semi-Annual Metabolic Monitoring
Participants will be monitored every six months for risk of type 1 diabetes
Related Therapeutic Areas
Sponsors
Collaborators: National Institute of Allergy and Infectious Diseases (NIAID), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), American Diabetes Association, National Center for Research Resources (NCRR)
Leads: University of South Florida

This content was sourced from clinicaltrials.gov