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Clinical Trials/CTRI/2012/04/002561
CTRI/2012/04/002561
Recruiting
未知

A comparative study of misoprostol oral versus vaginal route for induction of labour - Nil

AGMC and GBP Hospital Agartala0 sites130 target enrollmentTBD
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ConditionsHealth Condition 1: null- All fullterm pregnant patients having live singleton fetus with vertex presentation and Bishops less than score 5.

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- All fullterm pregnant patients having live singleton fetus with vertex presentation and Bishops less than score 5.
Sponsor
AGMC and GBP Hospital Agartala
Enrollment
130
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
AGMC and GBP Hospital Agartala

Eligibility Criteria

Inclusion Criteria

  • •1\.A live singleton pregnancy of \> 37 weeks for obstetric or medical indication for induction
  • •2\.Vertex presentation.
  • •3\.Prolonged pregnancy.
  • •4\.Bishop score less than 5\.
  • •5\.Intact membrane without previous stripping.

Exclusion Criteria

  • •1\.Suspected cephalo\-pelvic disproportion.
  • •2\.Previous caesarean section or history of uterine surgery.
  • •3\.Multiple gestations.
  • •4\.Malpresentation.
  • •5\.Any contraindication for vaginal delivery or prostaglandin administration and suspected chorioamnionitis.
  • •6\.Suspected fetal jeopardy.
  • •7\.Placenta previa.
  • •8\.Grand multigravida.

Outcomes

Primary Outcomes

Not specified

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