Guideline-directed Management and Therapy (GDMT) for the Prevention of Postpartum Cardiac Dysfunction in Preeclamptic African American Women (NCT05534932)

🧪 Interventions in This Study

• Remote Patient Monitoring (DEVICE)

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (1 Sites)

• University of Chicago Hospital — Chicago, Illinois

💰 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

• Sensitivity of Angiotensin II Type II Receptors in Women Following Preeclampsia — Iowa City, Iowa
• Aspirin for Postpartum Patients With Preeclampsia — Long Beach, California
• Aspirin and Preeclampsia — Chicago, Illinois
• Postpartum Low-Dose Aspirin and Preeclampsia — New York, New York

Explore by condition: All Preeclampsia Postpartum clinical trials

💡 How to Participate

1. Check the checklist above to see if you may qualify.
2. Review the official NIH record below to find the coordinating site.
3. Ask about the visit schedule, what is covered at no cost, and any travel support.
4. Confirm with your own doctor before making a decision.