drugset / Trial / NCT04343235

Postpartum Management of Gestational Hypertensive Disorders Using Furosemide

NCT04343235

Phase 4 Terminated 13 enrolled Wright State University
RandomizedParallel-groupOpen-labelTreatment

Summary

* The main purpose of this study is to learn if incorporating a loop diuretic such as furosemide along with labetalol in the routine management of postpartum gestational hypertensive disorders could lower the need for additional anti-hypertensive agents to control blood pressures, improve blood pressures (as measured by systolic blood pressure, diastolic blood pressure and mean arterial blood pressures), shorten hospital stays and decrease readmissions for patients with gestational hypertensive disorders. * Based on a study by Veena et al1, there is reason to believe that the addition of furosemide to other anti-hypertensives may help decrease the need to add or increase the dose of medication to control blood pressures. There may be potential to shorten hospital stays and decrease readmissions, as well. Collecting data will be done using a prospective, randomized 1:1 controlled study assigning postpartum patients with a gestational hypertensive diagnosis to either labetalol alone or labetalol plus furosemide. * The study will be performed in the postpartum wing of Miami Valley Hospital Main Campus and would use patients who have consented to participate in the study with enrollees coming from the OB Staff population.

Timeline

Start
2020-05-01
Primary completion
2022-06-30
Completion
2022-06-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Furosemide Other / unclassified 20 mg
Subject Labetalol Small molecule 200 mg