Effect of sublingual Misoprostol versus vaginal Misoprostol in labor induction success.
Phase 2
- Conditions
- labour induction.Precipitate labour
- Registration Number
- IRCT138903121096N3
- Lead Sponsor
- Vice chancellor for research -Guilan university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 126
Inclusion Criteria
a) single pregnancy (between 36 to 42 weeks), b) vertex presentation, c) intact fetal membrane, d) bishop score equal or less than four e) absence of uterus spontaneous contractions f) fetal weight less than 4000gr j) normal fetal heart rate h) cephalopelvic proportion Exclusion criteria: a) sensitivity to PGs b) previous history of cesarean c) uterus wall scar d) preeclampsia or blood pressure more than 140/90 mmhg e) PROM f) vaginal bleeding
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time interval from labour induction to delivery. Timepoint: After delivery. Method of measurement: Time recording of induction beginning and delivery in Questionnaire.;Delivery type frequency. Timepoint: After delivery. Method of measurement: patient medical document.;Dose amount. Timepoint: Four hours after last prescription of Misoprostol up to delivery time. Method of measurement: Patient medical document.
- Secondary Outcome Measures
Name Time Method