The Effect of vaginal wash with 3% acetic acid on the efficacy of vaginal misoprostol for labour induction at term at Federal Medical Centre, Abeokuta
Phase 1
Recruiting
- Conditions
- Pregnancy and Childbirth
- Registration Number
- PACTR202305754076736
- Lead Sponsor
- IMOTALLAH OJUGBELE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 96
Inclusion Criteria
•Pregnant women who have consented to participate in the study
•singleton pregnancy
•cephalic presentation
•term gestation (defined as =37 weeks)
•Normal fetal heart rate on cardiotocography
•Bishop score of =5
Exclusion Criteria
•Allergy to misoprostol
•Multiple pregnancies
•Gestational age < 37 weeks
•Malpresentation
•Estimated fetal weight of >4000 gm
•Ruptured membranes
•Non-reassuring cardiotocography
•=Para 4
•Nonconsenting women
•Fetal anomaly and fetal demise
•Previous uterine surgery
•Abnormal vaginal discharge
•Patients with vaginal pH = 5 with positive Whiff test
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Induction to delivery interval
- Secondary Outcome Measures
Name Time Method Interval Interval between induction and active phase of labour<br>The total dose of vaginal misoprostol that will achieve cervical ripening and induction of labour <br>The caesarean section rate, including the indication and outcome of the caesarean section <br>The occurrence of any feto-maternal complications<br> Interval between induction and active phase of labour<br>The total dose of vaginal misoprostol that will achieve cervical ripening and induction of labour <br>The caesarean section rate, including the indication and outcome of the caesarean section <br>The occurrence of any feto-maternal complications<br><br>