The comparison of drug and mechanical methods for cervical ripening before delivery

Not Applicable

• Conditions: O60-O75; Ripening Of Cervix.; Complications of labour and delivery

• Registration Number: IRCT201012225448N1
• Lead Sponsor: Tabriz University Of Medical Sciences? Vice chancellor for Research

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: 120

Inclusion Criteria

gestatinal age over 37 weeks, singleton gestation,cephalic presentation, intact amnion sac,not contraindication of misoprostol use,first gravity ,3 to 4 bishop score
Exclusion criteria:allergy to misoptostol,elective cesarean section,urgent delivery by c/s,IUGR,placenta previa,fetal bradycardia, placenta abruption,massive bleeding ,placenta previa and previous cesarean section.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Ripening of cervix. Timepoint: in the time of intervention. Method of measurement: bishop score.

Secondary Outcome Measures

Name	Time	Method
Meconium In Amnionic Fluid. Timepoint: at time of intervention. Method of measurement: Clinical.;Uterine Hyperstimulation. Timepoint: at time of intervention. Method of measurement: clinical.;Rupture of uterin. Timepoint: at time of intervention. Method of measurement: clinical.;Result in c/s. Timepoint: at time of intervention. Method of measurement: Clinical.;Fetal Bradycardia. Timepoint: In the time of intervention. Method of measurement: Clinical.