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Clinical Trials/IRCT20230611058454N1
IRCT20230611058454N1
Recruiting
Phase 3

Comparison of the effect of misoprostol alone and misoprostol together with vaginal estrogen in preparing the cervix and induction of labor in term pregnancies

Tehran University of Medical Sciences0 sites200 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Tehran University of Medical Sciences
Enrollment
200
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • Term pregnancy (Gestational age \>37 weeks)
  • Nulliparous woman
  • Singleton pregnancy
  • Alive Fetus with cephalic presentation
  • Bishop score \< 5

Exclusion Criteria

  • Misoprostol or estrogen contraindication
  • Women with a history the uterus surgery
  • Women with a history or family history of thromboembolism

Outcomes

Primary Outcomes

Not specified

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