Efficacy of oral MIFEPRISTONE for pre induction cervical ripening in term pregnancy
Not Applicable
- Registration Number
- CTRI/2023/09/057908
- Lead Sponsor
- Shri Dharmastala Manjunatheshwara College of Medical Sciences and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Primigravida, Cephalic presentation, between 37-42 weeks of gestation, unripe cervix ( bishop score <6), maternal age >18 years, at admission NST reactive, intact membranes.
Exclusion Criteria
Multigravida, contra indications for induction of labour, estimated fetal weight > 4.5 kg or <2.5 kg, antepartum haemorrhage, chorioamniotis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the efficacy of Mifepristone for pre induction cervical ripeningTimepoint: measured at baseline (after 24hours)
- Secondary Outcome Measures
Name Time Method To evaluate outcome of labour to study fetal & maternal complicationsTimepoint: after each delivery outcome measured at baseline