Comparison of vaginal misoprostol and intra cervical foleycatheter for cervical ripening

Not Applicable

• Conditions: Spontaneous delivery.; Encounter for full-term uncomplicated delivery; O80.0

• Registration Number: IRCT20181218042033N4
• Lead Sponsor: Bandare-abbas University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 18 May 2020

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 120

Inclusion Criteria

Primigravid women
18-35 yeares old
Vaginal bleeding
Abnormal fetal heartbeat
Natural disease that needed to terminate the pregnancy season

Exclusion Criteria

Misoprostol susceptibility
Uterine scar

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Cervical dilatation. Timepoint: Every 6 hours. Method of measurement: Vaginal examination.