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Clinical Trials/IRCT201402096541N3
IRCT201402096541N3CompletedPhase 2

Comparison of the efficacy and complications of sublingual versus vaginal misoprostol for induction of laborfor women in term pregnancy

Shiraz University of Medical Sciences- Vice Chancellor for Research0 sites200 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 2
Status
Completed
Sponsor
Enrollment
200

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 45 years (—)
Sex
Female

Inclusion Criteria

  • first singleton alive pregnancy; gestational age of =37 weeks: cephalic presentation: estimated fetal weight of less than 4000 grams; Bishop Score <7.
  • Exclusion criteria: : hypersensitivity to prostaglandins; previous uterine scar; fetal congenital malformations; intrauterine growth restriction; non-reassuring fetal heart; gestational age <37 weeks; oligohydramnious.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Shiraz University of Medical Sciences- Vice Chancellor for Research

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