Comparison of vaginal Misoprostol versus Foley catheter for labor inductio

Not Applicable

• Conditions: pregnancy.; Pregnancy, childbirth and the puerperium; O00-O99

• Registration Number: IRCT2017052710340N13
• Lead Sponsor: Vice chancellor for research, Golestan 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: 60

Inclusion Criteria

Cephalic presentation; healthy amnion; Bishop score less than 6; inappropriate cervix; inappropriate uterine contractions; normal fetal heart rate.
Exclusion criteria was considered as : Pelvic dystocia; fetal weight more than 4 kg; incompatibility of fetal head with maternal pelvis ; placenta praevia; unexplained vaginal bleeding; the parity more than five; fetal anomaly; previous uterine scar; any situation that makes vaginal delivery impossible.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
abor induction. Timepoint: The first, second and third phase of delivery. Method of measurement: Stopwatch.

Secondary Outcome Measures

Name	Time	Method
Apgar. Timepoint: The first minute after the baby is born. Method of measurement: Apgar score.;Bleeding. Timepoint: After delivery. Method of measurement: The number of bleeding pads.