Daily Aspirin Treatment After Preeclampsia
Part of paid clinical trials in Iowa City, Iowa.
- Sponsor
- Anna Stanhewicz, PhD
- Study ID
- NCT06168461
- Phase
- EARLY_PHASE1
- Status
- Recruiting
Conditions
- Preeclampsia
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 50 Years
- Healthy Volunteers
- Not accepted
Interventions
- Aspirin — DRUG162mg aspirin capsule
- Placebo — DRUGplacebo capsule
Study Details
Women who develop preeclampsia during pregnancy are four times more likely to develop cardiovascular disease later in life, even if they are otherwise healthy. The reason why this occurs may be related to lasting blood vessel damage after the pregnancy but there are currently no specific treatment strategies to prevent this disease progression. This study addresses this public health issue by examining whether starting low dose aspirin therapy after pregnancy is an effective treatment for lasting blood vessel damage in order to inform better clinical management of cardiovascular disease risk in women who have had preeclampsia.
Key Dates
- Start date
- Nov 1, 2023
- Status verified
- Dec 2025
- Primary completion
- Jun 30, 2026
- Completion
- Jun 30, 2026
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Placebo Comparator: placeboplacebo pill taken once daily at bedtime for 12 weeks
- Experimental: aspirin162mg aspirin taken once daily at bedtime for 12 weeks
Primary Outcome Measure
magnitude of microvascular endothelial function [ Time Frame: baseline, 12 weeks ]
Central Contacts
- Anna Reid-Stanhewicz, PHD319-467-1732
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Iowa | Iowa City | Iowa | 52242 |
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