PRO Development for ANCA Associated Vasculitis

NCT01729624 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2015-05-28

No results posted yet for this study

Summary

A qualitative study using interviews with patients who have antineutrophil cytoplasm antibody (ANCA) associated vasculitis, to develop a patient reported outcome (PRO)measure

Conditions

  • Wegener Granulomatosis
  • Microscopic Polyangiitis
  • Churg-Strauss Syndrome

Sponsors & Collaborators

  • University of Oxford

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-09-30
Primary Completion
2015-08-31
Completion
2015-08-31

Countries

  • United Kingdom

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 NCT01729624 on ClinicalTrials.gov