Oral versus vaginal administration of misoprostol for induction of labor in women with pre labour rupture of membranes. Results of a randomized controlled trial
Phase 4
Recruiting
- Conditions
- Premature rupture of membranes at term
- Registration Number
- JPRN-UMIN000039212
- Lead Sponsor
- JNMC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 51
Inclusion Criteria
Not provided
Exclusion Criteria
CD 4 BS 6
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome measure was to compare the effectiveness of orally administered misoprostol, with vaginally administered misoprostol for induction of labor in PROM cases.
- Secondary Outcome Measures
Name Time Method Secondary outcomes were evaluation of mean interval between induction and active labor and the Induction to delivery interval.