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Clinical Trials/IRCT2014061412789N3
IRCT2014061412789N3
Completed
未知

A comparison of vaginal and oral dose of misoprostol for labor induction in post-term pregnancies

Vice Chancellor for Research, Kurdistan University of Medical Sciences0 sites180 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Efficacy on induction of labor.
Sponsor
Vice Chancellor for Research, Kurdistan University of Medical Sciences
Enrollment
180
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Vice Chancellor for Research, Kurdistan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Gestational age (GA) greater or equal to 40 weeks and 6 days with cephalic presentation and Bishop score greater than 4 and a height of 150 cm. Exclusion criteria included contraindications to receive misoprostol (allergies, asthma, Pelvic Inflammatory Disease, Acute Cerebrovascular Disease, Coronary Artery Disease, seizures) and also placenta previa , history of previous cesarean section or uterine surgery, Cephalopelvic Disproportion , Bishop score greater than 4, and abnormal vaginal bleeding.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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