RANDOMIZED COMPARISON OF 2 DRUGS FOR CERVICAL RIPENING IN TERM PREGNANCY
Phase 2
Completed
- Conditions
- Health Condition 1: null- PRE- INDUCTION CERVICAL RIPENING IN TERM PREGNANCY
- Registration Number
- CTRI/2013/07/003808
- Lead Sponsor
- safdarjung hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 500
Inclusion Criteria
37 completed weeks of gestation, Singleton fetus, Cephalic presentation, Absence of uterine contractions, Unfavorable cervix (Bishop <6), Intact membranes, Reactive NST
Exclusion Criteria
Fetal malpresentation, Antepartum hemorrhage, Previous uterine incision, Ruptured membranes, Contraindication to receive IMN or Prostaglandins(allergy, bronchial asthma, hypotension, palpitation), Severe anemia, Heart disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method