Induction of labor with 3 different methods.

Phase 2

• Conditions: Condition 1: Delivery. Condition 2: Outcome of delivery.; Pregnancy, childbirth and the puerperium; Outcome of delivery; O00-O99

• Registration Number: IRCT201702282624N22
• Lead Sponsor: Vice chancellor for research ,Iran University of Medical Sciences.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 116

Inclusion Criteria

Inclusion criteria : maternal age between 18-40 years old; gestational age of more than 37 weeks ; singleton, cephalic presentation, intact membrane and Bishop Score of less than 6. Exclusion criteria : any sign of fetal distress; placenta previa and any vaginal bleeding of more than bloody show; history of any surgery on uterus including cesarean section; known uterine anomaly; intra uterine fetal death, and known hypersensitivity to misoprostol.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Delivery during the first 24 hours after intervention. Timepoint: 24 hours. Method of measurement: Data sheets.

Secondary Outcome Measures

Name	Time	Method
Duration of the stages of labor. Timepoint: 1 hour. Method of measurement: Data sheets.;The adverse effects in mothers. Timepoint: each hour. Method of measurement: Data sheets.;The adverse effects in neonates. Timepoint: After birth up to discharge. Method of measurement: Data sheets.