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CompletedNCT01108289

Effect of Prophylactic Administration of Oxytocin in Uniject™ on Postpartum Hemorrhage at Home Births in Ghana

The Oxytocin Initiative: Determining the Effect of Prophylactic Administration of Oxytocin in Uniject™ by a Community Health Officer on Postpartum Hemorrhage at Home Births in Four Districts in Ghana

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,586 (actual)
Sponsor
Johns Hopkins Bloomberg School of Public Health · Academic / Other
Sex
Female
Age
15 Years – 50 Years
Healthy volunteers
Accepted

Summary

This study is designed to test the hypothesis that the intramuscular administration of 10 IU of oxytocin in Uniject™ during the third stage of labor by a Community Health Officer (CHO) at home births in Ghana will reduce the risk of postpartum hemorrhage by 50 percent relative to home births attended by the same type of provider who does not provide a uterotonic drug.

Conditions

Interventions

TypeNameDescription
OTHEROxytocin in Uniject10 IU Oxytocin delivered intramuscularly immediately after delivery of the baby

Timeline

Start date
2011-04-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2010-04-21
Last updated
2013-07-02

Locations

1 site across 1 country: Ghana

Source: ClinicalTrials.gov record NCT01108289. Inclusion in this directory is not an endorsement.

Effect of Prophylactic Administration of Oxytocin in Uniject™ on Postpartum Hemorrhage at Home Births in Ghana (NCT01108289) · Clinical Trials Directory