Clinical Trials Directory

Trials / Completed

CompletedNCT01608958

IV vs IM Oxytocin in the Third Stage of Labor for Prevention of Postpartum Hemorrhage

Intravenous and Intramuscular Administration of Oxytocin in the Third Stage of Labor for Prevention of Postpartum Hemorrhage

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
653 (actual)
Sponsor
Gynuity Health Projects · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

The study will evaluate whether prophylactic oxytocin administered in the third stage of labor via IV infusion results in a lower mean blood loss compared to IM injection.

Detailed description

The study will compare the effect of IV infusion and IM oxytocin administration on the proportion of women who experience blood loss greater than or equal t 350 ml, the proportion of women who experience blood loss greater than or equal to 500 ml, side effects, adverse events and change in hemoglobin pre- to post-delivery. It will also assess whether a bleeding history questionnaire can identify women at risk for excessive bleeding and help to define the distribution of bleeding scores among women with and without excessive bleeding.

Conditions

Interventions

TypeNameDescription
DRUGOxytocin10 IU oxytocin in 500 ml infusion
DRUGOxytocin10 IU oxytocin IM injection

Timeline

Start date
2012-05-01
Primary completion
2012-11-01
Completion
2012-12-01
First posted
2012-05-31
Last updated
2016-03-28

Locations

3 sites across 3 countries: Ecuador, Turkey (Türkiye), Vietnam

Source: ClinicalTrials.gov record NCT01608958. Inclusion in this directory is not an endorsement.