drugset / Trial / NCT02989025

Progesterone to Enhance the Efficacy and Success of Expectantly Managed Preterm Severe/Superimposed Preeclampsia

NCT02989025

Phase 2 Recruiting 60 enrolled University of Mississippi Medical Center
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to learn if giving 17-hydroxyprogesterone caproate (17 OHPC) to mothers with preeclampsia diagnosed before 34 weeks gestation improves mother and baby outcomes.

Timeline

Start
2017-05-22
Primary completion
2027-01-31
Completion
2027-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject 17-alpha-hydroxyprogesterone caproate Unknown 250 mg Intramuscular

Indications