Vasculitis Pregnancy Registry

ConditionsVasculitis Behcet's Disease CNS Vasculitis Cryoglobulinemic Vasculitis Eosinophilic Granulomatosis With Polyangiitis (EGPA)Churg-Strauss Syndrome (CSS)Granulomatosis With Polyangiitis (GPA)Wegener's Granulomatosis IgA Vasculitis Henoch-Schoenlein Purpura (HSP)Microscopic Polyangiitis (MPA)Polyarteritis Nodosa (PAN)Takayasu Arteritis (TAK)Urticarial Vasculitis Systemic Vasculitis

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexFemale

Age18-50

SponsorUniversity of Pennsylvania

About this trial

The purpose of this study is to learn about the experience of women with vasculitis who become pregnant. In particular, the study will consist of several online surveys to assess

1. each woman's vasculitis severity and pregnancy-related experiences, and 2. pregnancy outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Behçet's disease;

Central nervous system (CNS) vasculitis;

Cryoglobulinemic vasculitis (Cryoglobulinemia);

Eosinophilic granulomatosis with polyangiitis (also called Churg-Strauss Syndrome);

Disqualifiers

Non-English speaking, with the exception of people who speak Spanish, Portuguese, Italian, or Turkish.

Unable to provide consent.

Trial population

Women with vasculitis who are currently pregnant.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Online questionnaires
Other intervention
Women will be asked to complete questionnaires during their pregnancy and a postpartum questionnaire.

Treatment groups

100 Participants

are divided into 1 treatment group

Group A: Intervention1 intervention

Trial outcomes

Primary outcomes

Unique pregnancy characteristics among women with vasculitis.

To understand pregnancy characteristics and outcomes among women with vasculitis using patient-reported questionnaires in each trimester.

Time frame

Four years

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Pennsylvania

Lead sponsor

Duke University

Collaborator

University of South Florida

Collaborator

Source ClinicalTrials.gov

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