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Effect of misoprostol on labor

Not Applicable
Conditions
Efficacy on induction of labor.
Failed medical induction of labour
Registration Number
IRCT201202018897N1
Lead Sponsor
Faculty of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
102
Inclusion Criteria

singleton live pregnancy at term(GA= 37week) in the cephalic presentation; absent of active labor; unfavorable cervix(Bishop scor=6) and normal fetal heart rate tracing.
Exclusion criteria: known cephalopelvic disproportion; abnormal presentation; previous cesarean delivery or other type of uterine surgery; cervical cancer; fetal macrosomia; active herpes genitalia; multiparity and fetal anomaly.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Interval from induction to true labor. Timepoint: Vaginal exam for evaluation of dilatation and effacment. Method of measurement: By vaginal exam.;Interval from true labor to delivery. Timepoint: Vaginal exam for evaluation of dilatation and effacment q 1 hour. Method of measurement: By vaginal exam.;Interval from induction to delivery. Timepoint: Vaginal exam for evaluation of dilatation and effacment q 1 hour. Method of measurement: By vaginal exam.
Secondary Outcome Measures
NameTimeMethod
Rate of vaginal delivery. Timepoint: At delivery time and 48 hours afterthat. Method of measurement: By clinical evaluation and add to form.;Post partum complication. Timepoint: At delivery time and 48 hours afterthat. Method of measurement: By clinical evaluation and add to form.;Neonatal outcom. Timepoint: At delivery time and 48 hours afterthat. Method of measurement: By clinical evaluation and add to form.
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