Comparison of the safety and efficacy of labor induction with oral Misoprostol in different doses

Phase 4

• Conditions: Preterm Premature Rupture of Membrane.; Preterm premature rupture of membranes, unspecified as to length of time between rupture and onset of labor; O42.91

• Registration Number: IRCT20221123056587N1
• Lead Sponsor: Iran 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: Complete
• Sex: Female
• Target Recruitment: 400

Inclusion Criteria

Pregnant women with premature rupture of membranes
No history of cesarean delivery
No Contraindication of natural labor
No Contraindication to Misoprostol
Cephalic presentation
Parity less than 5
Bishop Score of less than 4
Singleton pregnancy
Pregnant for 36 weeks or more

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time Interval Between the beginning of Labour Induction and Occurrence of the Labour. Timepoint: Time Interval Between the beginning of Labour Induction and Occurrence of the Labour. Method of measurement: Timing.;Health of the newborn. Timepoint: Between minute one to minute five after the birth. Method of measurement: Apgar score.;Type of Labour. Timepoint: At the time of the birth. Method of measurement: Observation.