Eosinophilic Granulomatosis With Polyangiitis Cohort
NCT03036670 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50
Last updated 2023-04-07
Summary
EGPA (Eosinophilic Granulomatosis with Polyangiitis, previously Churg-Strauss syndrome) is a rare vasculitis, characterised by asthma, rhinosinusitis and eosinophilia. There has previously been confusion around diagnostic criteria, with multiple sets of classification criteria being used inappropriately for diagnosis. The ERS formed a taskforce to produce specific diagnostic criteria, and these divided the Churg-Strauss Syndrome cohort into two groups - vasculitic EGPA and tissular Hypereosinophilic Asthma with Systemic Manifestations (HASM). It is not known if the groups separated by the diagnostic criteria are also separated in clinical symptomatology, or if their disease course varies, and this could have significant impact on management and further research.
Conditions
- Churg-Strauss Syndrome
Sponsors & Collaborators
-
Portsmouth Hospitals NHS Trust
lead OTHER_GOV
Principal Investigators
-
Anoop J Chauhan, PhD FRCP · Portsmouth Hospitals NHS Trust
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-08-10
- Primary Completion
- 2017-01-31
- Completion
- 2017-01-31
Countries
- United Kingdom
Study Locations
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