VCRC Patient Contact Registry Patient-Reported Data Validation Study

Completed

Conditions studied: Behcet's Disease, Churg-Strauss Syndrome, Giant Cell Arteritis, Wegener Granulomatosis, Microscopic Polyangiitis, Polyarteritis Nodosa, Takayasu's Arteritis

In brief

The purpose of this study is to provide validation of patient-reported data in the VCRC Patient Contact Registry by comparing patient-reported data with data provided by the physician who is the primary provider caring for the patient's vasculitis. Patients enrolled in the Patient Contact Registry with Behcet's disease, eosinophilic granulomatosis with polyangiitis (Churg-Strauss) (EGPA), giant cell arteritis (GCA), granulomatosis with polyangiitis (Wegener's) (GPA), microscopic polyangiitis (MPA), polyarteritis nodosa (PAN), and Takayasu's arteritis (TAK) were invited via email to participate in this study.

Key facts

Study ID

NCT02190942

Run by

University of South Florida

People needed

198

Starts

2014-05-01

Expected to finish

2019-06-18

Last updated by the study team

2019-10-16

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• At least 20 patients with each of the following self-identified diagnoses in the VCRC Patient Contact Registry: Behçet's disease, EGPA, GCA, GPA, MPA, PAN, and TAK who have completed the online questionnaires.

You may not qualify if…

• Inability to provide informed consent and complete survey
• Patients whose diagnosis of vasculitis was not confirmed by a physician
• Patients who did not complete the initial questionnaire in its entirety

Where it is running

• University of South Florida Data Management Coordinating Center — Tampa, Florida, United States

Full record on ClinicalTrials.gov

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