NCT03556761View on ClinicalTrials.gov

Furosemide for Accelerated Recovery of Blood Pressure Postpartum

PHASE2CompletedINTERVENTIONAL
Enrollment

384

Participants

Timeline

Start Date

June 20, 2018

Primary Completion Date

December 4, 2019

Study Completion Date

February 5, 2020

Conditions
Hypertension, Pregnancy-Induced
Interventions
DRUG

Oral furosemide

Furosemide (Lasix), 20 milligram, PO, PO, daily

DRUG

Placebo Oral Tablet

Placebo, PO, daily

Trial Locations (1)

19104

Hospital of the University of Pennsylvania, Philadelphia

All Listed Sponsors
lead

University of Pennsylvania

OTHER

NCT03556761 - Furosemide for Accelerated Recovery of Blood Pressure Postpartum | Biotech Hunter | Biotech Hunter