Trial intelligence / Profile preview

Efficacy of Postpartum Furosemide in Patients With Severe Preeclampsia

NCT07861685Recruiting

Start
Oct 2026
Primary completion
Mar 2027
Countries
1
01

Overview

Randomised, double-blind trial in preeclampsia comparing Furosemide Group with Placebo Group (2 arms). Primary endpoint: Blood Pressure at 7 days. Started Oct 2026; status: recruiting.

02

Drugs

furosemide
03

Conditions

preeclampsia

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