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Postpartum Hemorrhage Prevention in Patients With Preeclampsia (PHP3 Study) — PHP3  

Preeclampsia Clinical Trial

Official title:
Postpartum Hemorrhage Prevention in Patients With Preeclampsia (PHP3 Study)

Clinical Trial Summary

Evaluation of the efficacy of postpartum 24 hour oxytocin infusion to reduce blood loss in patients with pre-eclampsia (PE)

Clinical Trial Description

The overall goal of this study is to evaluate the efficacy of postpartum 24 hour oxytocin infusion as a prevention-oriented strategy to reduce blood loss in patients with pre-eclampsia (PE) in a blinded, placebo controlled, randomized controlled trial. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02221830
Study type Interventional
Source University of Colorado, Denver
Contact
Status Completed
Phase Early Phase 1
Start date February 2015
Completion date July 17, 2019
View Details
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