Aspirin and Preeclampsia (NCT04479072)
Aspirin to Prevent Cardiac Dysfunction in Preeclampsia
🩺 Plain-English Summary (8th-Grade Level)
This is a single-center, double-blind, randomized, placebo-controlled clinical trial. Peripartum and postpartum Activin A are significantly elevated in women with preeclampsia. Our hypothesis is that elevated Activin A levels reflect a remediable signal and that reducing postpartum Activin A levels with aspirin therapy will improve (GLS) in preeclamptic patients.
Who can join: Review the eligibility criteria below.
Location: University of Chicago Hospital — Chicago, Illinois
Age range: 18 Years to 45 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- University of Chicago Hospital — Chicago, Illinois
📞 Contact the Study Coordinator
Phone: (773) 398-2956
Email: sshahul1@dacc.uchicago.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Preeclampsia Postpartum
- Guideline-directed Management and Therapy (GDMT) for the Prevention of Postpartum Cardiac Dysfunction in Preeclamptic African American Women — Chicago, Illinois
- Sensitivity of Angiotensin II Type II Receptors in Women Following Preeclampsia — Iowa City, Iowa
- Aspirin for Postpartum Patients With Preeclampsia — Long Beach, California
- Postpartum Low-Dose Aspirin and Preeclampsia — New York, New York
Explore by condition: All Preeclampsia Postpartum clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.