abor induction in term pregnant women of with oral misoprostol or oxytoci

Early Phase 1

Conditions: labor induction.
Pregnancy with abortive outcome
O00-O08

Registration Number: IRCT2012061910068N1

Lead Sponsor: Shahid Beheshti University of Medical Science

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: Female

Target Recruitment: 285

Inclusion Criteria

term pregnant women whom were candidate for vaginal delivery; gestational age of 38 to 42 weeks; birth weight of maximally 4000 grams; normal fetal heart rate; cephalic presentation; lack of uterine contractures; single pregnancy and Bishop Score of six and less.
The exclusion criteria were lack of satisfaction for incorporation in the study; having a positive history of uterine surgery including cesarean; intrauterine growth retardation (IUGR); oligohydramnios; placenta previa; umbilical cord prolapse; active herpes infection; symptoms of chorioamnionitis; hepatic or renal disease; non-reactive contraindications for prostaglandins use; contraindications for labor induction and idiopathic vaginal bleeding.

Exclusion Criteria

Not provided

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The time from induction to delivery. Timepoint: 12, 18, and 24 hours during labor. Method of measurement: Data recording.;The time from induction to the beginning of the active phase. Timepoint: 12, 18, and 24 hours during labor. Method of measurement: Data recording.;Mode of delivery. Timepoint: 12, 18, and 24 hours during labor. Method of measurement: Data recording.

Secondary Outcome Measures

Name	Time	Method
Maternal complications. Timepoint: Peri labor phase. Method of measurement: Data record.;Fetal and neonatal status. Timepoint: Peri labor phase. Method of measurement: Data record.