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VCRC Patient Contact Registry Patient-Reported Data Validation Study

NCT02190942 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 198

Last updated 2019-10-16

No results posted yet for this study

Summary

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.

Conditions

  • Behcet's Disease
  • Churg-Strauss Syndrome
  • Giant Cell Arteritis
  • Wegener Granulomatosis
  • Microscopic Polyangiitis
  • Polyarteritis Nodosa
  • Takayasu's Arteritis

Sponsors & Collaborators

  • Wayne State University

    collaborator OTHER

  • University of Pittsburgh

    collaborator OTHER

  • University of Pennsylvania

    collaborator OTHER

  • Boston University

    collaborator OTHER

  • University of South Florida

    lead OTHER

Principal Investigators

  • Kathleen McKinnon, DO · Henry Ford/Wayne State University

  • Ximena D. Ruiz, MD · University of Pittsburgh

  • Peter A. Merkel, MD, MPH · University of Pennsylvania

  • Jennifer L. Harris, MSPH, CCRP · University of South Florida

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-05-31
Primary Completion
2017-12-01
Completion
2019-06-18

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02190942 on ClinicalTrials.gov