RecruitingNCT02593565

Vasculitis Pregnancy Registry

The Vasculitis Pregnancy Registry (V-PREG)


Sponsor

University of Pennsylvania

Enrollment

100 participants

Start Date

Nov 1, 2015

Study Type

OBSERVATIONAL

Conditions

Summary

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

Sex: FEMALEMin Age: 18 YearsMax Age: 50 Years

Plain Language Summary

Simplified for easier understanding

The Vasculitis Pregnancy Registry collects information about pregnancies in women who have vasculitis — a group of conditions where the immune system attacks blood vessels, causing inflammation. Because these conditions are rare and little is known about how they interact with pregnancy, this registry aims to gather data that could help doctors better care for pregnant women with vasculitis in the future. You may be eligible if: - You are a woman aged 18 to 50 - You are currently pregnant - You have been diagnosed with one of the following: Behçet's disease, CNS vasculitis, Cryoglobulinemic vasculitis, Eosinophilic granulomatosis with polyangiitis (Churg-Strauss), Giant Cell Arteritis, Granulomatosis with polyangiitis (Wegener's), IgA vasculitis (Henoch-Schoenlein purpura), Microscopic polyangiitis, Polyarteritis nodosa, Takayasu's arteritis, Urticarial vasculitis, or suspected vasculitis - You speak English, Spanish, Portuguese, Italian, or Turkish You may NOT be eligible if: - You speak a language other than those listed above - You are unable to provide consent Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHEROnline questionnaires

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


Locations(1)

University of South Florida Data Management and Coordinating Center

Tampa, Florida, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT02593565


Related Trials