Scleroderma Registry

Completed

Conditions studied: Systemic Sclerosis, Scleroderma

In brief

Scleroderma is likely caused by a combination of factors, including an external trigger (infection or other exposure) and a genetic predisposition. The Scleroderma Registry will conduct genetic analyses for disease-related genes in patients with scleroderma and their family members (parents, brothers, and sisters).

Key facts

Study ID

NCT00074568

Run by

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

People needed

5000

Starts

2000-09-01

Expected to finish

2022-01-01

Last updated by the study team

2022-09-27

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Diagnosis of systemic sclerosis or family members of patients with systemic sclerosis
• Or
• Healthy volunteer with no autoimmune disease and without a first-degree relative with a systemic autoimmune disease

Where it is running

• University of Texas - Houston Medical School — Houston, Texas, United States

Full record on ClinicalTrials.gov

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