drugset / Trial / NCT07648251

Furosemide vs Placebo in Severe Preeclampsia Postpartum

NCT07648251

Phase 2 Not yet recruiting 186 enrolled Universidad Nacional Autonoma de Honduras
RandomizedParallel-groupTriple-blindTreatment

Summary

This randomized, double-blind, placebo-controlled trial evaluates whether oral furosemide 40 mg, initiated 12 hours postpartum, reduces hospital length of stay compared to placebo (folic acid 5 mg) in postpartum women with severe preeclampsia. Secondary outcomes include need for rescue antihypertensive medications, weight reduction, and metabolic safety (hypokalemia, renal function). A total of 186 participants (93 per arm) will be enrolled across two hospitals in Honduras.

Timeline

Start
2026-06-15
Primary completion
2026-12-31
Completion
2027-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Furosemide Other / unclassified 40 mg Oral

Indications