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Clinical Trials/PACTR201802003154375
PACTR201802003154375
Completed
未知

A randomized clinical trial of sublingual versus rectal misoprostol for the prevention of postpartum hemorrhage in low resource settings

Faculty of Medicine0 sites600 target enrollmentFebruary 27, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Faculty of Medicine
Enrollment
600
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 27, 2018
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Faculty of Medicine

Eligibility Criteria

Inclusion Criteria

  • Pregnant women at term in active labour admitted to delivery room, with singleton pregnancy, vertex presentations with no risk factors for postpartum hemorrhage.

Exclusion Criteria

  • Grand multipara, operative vaginal delivery, previous uterine scar, contraindication to misoprostol or any risk factor for postpartum hemorrhage as multiple pregnancy, polyhydramnios and fetal macrosomia.

Outcomes

Primary Outcomes

Not specified

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