Clinical Trials Directory

Trials / Completed

CompletedNCT01863706

Misoprostol Versus Oxytocin for Prevention of Post Partum Hemorrhage

Safety and Efficacy of Misoprostol Versus Oxytocin for Prevention of Post Partum Hemorrhage

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
400 (estimated)
Sponsor
Hormozgan University of Medical Sciences · Academic / Other
Sex
Female
Age
10 Years – 50 Years
Healthy volunteers
Accepted

Summary

Post partum Hemorrhage (PPH) is one of three main causes of death in pregnant women. Oxytocin is widely used for prevention of PPH. Some studies suggested misoprostol as an alternative treatment when Oxytocin isn't available. The aim of this study is to compare the safety and efficacy of Oxytocin and misoprostol for prevention of PPH.

Detailed description

In a double blind randomized controlled trial 400 pregnant women who has vaginal delivery at Shariati hospital are assigned into two groups either to receive 20 unite oxytocin in 1000cc ringer and 2 placebo tablet or 400mcg oral misoprostol and 2cc normal saline in 1000cc ringer.

Conditions

Interventions

TypeNameDescription
DRUGMisoprostol400µg oral misoprostol
DRUGOxytocin20 IU Oxytocin

Timeline

Start date
2013-05-01
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2013-05-29
Last updated
2015-03-26

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT01863706. Inclusion in this directory is not an endorsement.