Comparison of Tansvaginal Ultrasound findings with Per Vaginal digital Examination Before Labour Induction for Successful Prediction of Induction of labour
Not Applicable
Completed
- Conditions
- Health Condition 1: O610- Failed medical induction of labor
- Registration Number
- CTRI/2023/03/050520
- Lead Sponsor
- Government medical college and hospital-32
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 299
Inclusion Criteria
1) Primigravida with singleton pregnancy with Cephalic presentation between 34-42 Weeks gestation.
2) Multiparty with present pregnancy first reach period of gestation at 34 weeks or above with singleton pregnancy with Cephalic presentation
Exclusion Criteria
1) IUGR( estimated birth weight- <1.5 kg to >3.5kg
2) Fetal Malprsentation
3) Multifetal Gestation
4) In Previous Prenancies Cesarean delivery or other uterine surgery ( Myomectomy, Hysterectomy)
5) Contraindications to Prostaglandin
6) Patient Refusing Consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Successful Normal Vaginal delivery of baby after Induction of labourTimepoint: 24 hours of prostaglandin administration and 12 hours of oxytocin infusion during labour induction
- Secondary Outcome Measures
Name Time Method Failure of induction and need of cesareanTimepoint: Inability to achieve active phase of labour after 24 hours of prostaglandin administration or and 12 hours of oxytocin infusion