The effect of misoprostol alone and misoprostol together with vaginal estrogen in induction of labor

Phase 3

Recruiting

• Conditions: abor induction.; Failed medical induction of labor; O61.0

• Registration Number: IRCT20230611058454N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 August 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 200

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Interval from induction with misoprostol to the attainment of 6 cm cervical dilation. Timepoint: Once, after delivery. Method of measurement: Information entered in the patient's delivery record.;Interval from 6 cm cervical dilation to full cervical dilation. Timepoint: Once, after delivery. Method of measurement: Information entered in the patient's delivery record.;Interval from full cervical dilation to active phase of labor. Timepoint: Once, after delivery. Method of measurement: Information entered in the patient's delivery record.