OPMIS

Not Applicable

• Conditions: Pregnancy and Childbirth; POST PARTUM HAEMORRHAGE

• Registration Number: PACTR201302000466116
• Lead Sponsor: PACE

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-11-27
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 4500

Inclusion Criteria

At the individual level, the study included pregnant women at 28 weeks (7months) or more of gestation determined from LNMP or clinical examination, had to be residents of Mubende or Mityana districts, above 18 years of age and anticipating uncomplicated vaginal delivery. Only women who gave informed written consent were included in the study. At the cluster level, the study included parishes projected to have at least 100 births within the study period.

Exclusion Criteria

The study excluded pregnant women with diagnosed multiple pregnancy,
chronic medical conditions
and reported hypersensitivity to prostaglandins or inability to give informed consent (e.g. mental health illness), as assessed by the recruiting research assistant

Study & Design

• Study Type: Interventional
• Study Design: Not specified