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NCT02887495 Clinical Trial

The Scleroderma Biorepository and Pathogenesis Study (STOP Scleroderma)

Scleroderma Clinical Trial

Official title:
The Scleroderma Biorepository and Pathogenesis Study (STOP Scleroderma)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02887495
Other study ID # 051427
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 2014
Est. completion date February 2, 2022

Study information
Verified date July 2022
Source George Washington University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Scleroderma bioreposiTOry and Pathogenesis Study (STOP Scleroderma) will help researchers use clinical data and human biospecimens to investigate why scleroderma patients develop certain complications from their disease. Patients with confirmed scleroderma, raynauds or positive autoantibodies are invited to participate. This research may help us understand how to prevent and treat scleroderma and other diseases.

Recruitment information / eligibility
Status Completed
Enrollment 600
Est. completion date February 2, 2022
Est. primary completion date February 2, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Age >18 years - Able to give informed consent. - Diagnosed with scleroderma or with positive autoantibodies Exclusion Criteria: - < 18 years old

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Victoria K Shanmugam Washington District of Columbia

Sponsors (1)
Lead Sponsor Collaborator
George Washington University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Modified Rodnan Skin Score 10 years
Secondary Medsger Severity Score 10 years
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