drugset / Trial / NCT07861685

Role of Postpartum Furosemide in Recovery of Patients With Severe Preeclampsia

NCT07861685 ↗

Recruiting 434 enrolled Lady Reading Hospital, Pakistan
RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized controlled trial will compare oral furosemide with placebo for improving blood pressure control in women with severe preeclampsia after delivery. Participants will receive either 20 mg of furosemide or a placebo tablet once daily for 5 days, in addition to standard postpartum treatment for high blood pressure. Blood pressure, symptoms, adverse events, and the need for additional antihypertensive medication will be monitored for 7 days after delivery. The study will assess whether adding furosemide helps achieve better postpartum blood pressure control compared with placebo.

Timeline

Start
2026-10-01
Primary completion
2027-03-15
Completion
2027-05-25

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Furosemide Other / unclassified 20 mg Oral
Background Potassium Small molecule — —

Indications