Comparison the effect of vaginal isosorbide dinitrate in pre-induction cervical ripening in term pregnancy

Phase 2

Recruiting

• Conditions: Pregnancy.; Normal pregnancy

• Registration Number: IRCT20130812014333N90
• Lead Sponsor: Kermanshah University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 May 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 148

Inclusion Criteria

Gestational age 37 weeks up to the end of the week
Cephalic presentation
No contraindications for isosorbide dinitrate
Normal body volume index (BMI = 19.8-26),
No history of previous cesarean section or any uterine scar

Exclusion Criteria

The presence of systemic diseases
Estimate fetal weight more than 4 kg
Vaginal bleeding
Intolerance to ISDN, labor pain and oligohydramnios

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Headache. Timepoint: At the beginning of the study, every 15 minutes to 1 hour, then every 30 minutes to 2 hours, and every 1 hour until delivery. Method of measurement: Ask the patient.;Nausea. Timepoint: At the beginning of the study, every 15 minutes to 1 hour, then every 30 minutes to 2 hours, and every 1 hour until delivery. Method of measurement: Ask the patient.;Blood pressure drop. Timepoint: At the beginning of the study, every 15 minutes to 1 hour, then every 30 minutes to 2 hours, and every 1 hour until delivery. Method of measurement: Sphygmomanometer.