Juvenile Rheumatoid Arthritis Research Registry
Recruitment status was: Recruiting
|Juvenile Rheumatoid Arthritis|
|Study Design:||Observational Model: Family-Based
Time Perspective: Prospective
|Official Title:||Research Registry for Juvenile Arthritis|
|Study Start Date:||October 1994|
|Estimated Primary Completion Date:||September 2009 (Final data collection date for primary outcome measure)|
Two or more biological siblings affected with JIA.
JRA is the most common chronic inflammatory pediatric rheumatic disease. JRA may be related to a complex genetic trait. It is rare to have two or more affected siblings, or sibpairs, within one family. The JRA ASP (Affected Sibpair) Registry is a nationwide effort and will collect information and blood samples from JRA sibpairs and their families. Unaffected family members (e.g., mother, father, and unaffected children) are also invited to participate.
Patients and their families may enroll in the registry in one of two ways: patients may contact the registry directly, or they may be referred to the registry through their physician. Once the family has qualified to join the registry, the family will be asked to complete a questionnaire on the medical history of their JRA-affected members. Physicians of the JRA-affected members will be asked to complete questionnaires about their patients' conditions. Family members will also be invited to provide a one-time blood sample. Information collected through the registry will help researchers identify genes involved in JRA susceptibility.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00090571
|Contact: Sandy Kramer, CRCemail@example.com|
|United States, Ohio|
|Cincinnati Children's Hospital Medical Center||Recruiting|
|Cincinnati, Ohio, United States, 45229-3039|
|Principal Investigator: David N. Glass, MD|
|Principal Investigator:||David N. Glass, MD||Children's Hospital Medical Center, Cincinnati|