Reproductive Outcomes for Women With Vasculitis.
Catherine A Sims, Amanda M Eudy, Kalen Larson...
https://pubmed.ncbi.nlm.nih.gov/38825354Actively Recruiting
Age: 18Years - 50Years
FEMALE
ID02593565
The Vasculitis Pregnancy Registry (V-PREG)
Led by University of Pennsylvania · Updated on 2026-01-23
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Pennsylvania
Lead Sponsor
D
Duke University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to understand the experiences of women with vasculitis who become pregnant. It focuses on assessing the severity of their vasculitis, their pregnancy-related experiences, and the outcomes of their pregnancies. The study is observational and seeks to gather detailed information through surveys over time. Women aged 18 to 50 years who have a diagnosis of vasculitis and are currently pregnant will be invited to participate. They will complete online questionnaires at several points: at study entry, during the second trimester, the third trimester, and after giving birth. These surveys take about 20 minutes each and are available in multiple languages including Spanish, Portuguese, Italian, and Turkish. Participants will provide information through these surveys, which will be securely stored and later analyzed by the study team. The main outcome measured is the unique pregnancy characteristics among women with vasculitis over a four-year period. This research involves no in-person visits and allows participants to contribute from home through their online responses.
CONDITIONS
Brief Title
Vasculitis Pregnancy Registry
Who Can Participate
Age: 18Years - 50Years
FEMALE
Eligibility Criteria
You may qualify if you...
- Women 18 years of age or older
- Diagnosis of one of the following diseases: Behcet's disease, CNS vasculitis, Cryoglobulinemic vasculitis, Eosinophilic granulomatosis with polyangiitis (Churg-Strauss Syndrome), Giant Cell (Temporal) Arteritis, Granulomatosis with polyangiitis (Wegener's), IgA vasculitis (Henoch-Schoenlein purpura), Microscopic polyangiitis, Polyarteritis nodosa, Takayasu's arteritis, Urticarial vasculitis, or Other/Suspected Diagnosis
- Currently pregnant (self-reported) at the time of enrollment
- Ability to provide consent
You will not qualify if you...
- Non-English speaking, except for those who speak Spanish, Portuguese, Italian, or Turkish
- Unable to provide consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
1
2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (online)
Monitoring
Duration - From enrollment through postpartum period (up to approximately 9 months or longer)
Participants complete online questionnaires to assess vasculitis severity, pregnancy experiences, and outcomes during pregnancy and postpartum.
4 online surveys: at study entry, second trimester, third trimester, and postpartum
Trial Site Locations
Total: 1 location
1
University of South Florida Data Management and Coordinating Center
Tampa, Florida, United States, 33612
Actively Recruiting
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Research Team
C
Christine Yeung
C
Carol McAlear, MA
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Published Research Related To This Trial
Exploring Reproductive Experiences With Women Enrolled in the International Vasculitis Pregnancy Registry.
Catherine A Sims, Brian Perry, Christine Yeung...
https://pubmed.ncbi.nlm.nih.gov/38825350