A study to compare two methods of inducing labour in full term pregnancy
Not Applicable
- Conditions
- Induction of labour
- Registration Number
- SLCTR/2014/001
- Lead Sponsor
- Teaching Hospital Mahamodara ,Galle
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
1.Women with singleton uncomplicated pregnancy
2.40 weeks of gestation with reliable pregnancy dating by ultrasound scan
3.Cephalic presentation
4.Unfavourable cervix (MBS<4)
5.Aged 18 years and above
6.No contraindication to vaginal delivery
.
Exclusion Criteria
1.Any medical complications (e.g. Pregnancy Induced Hypertension, Gestational Diabetes Mellitus)
2.Planned caesarean section
3.Fetal Growth Restriction
4.Past caesarian section
5.Fetal anomalies
6.Polyhydroamniosis or oligohydroamniosis
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in modified bishops score (MBS)<br><br><br> [At 40 week+6days of gestation .]<br>
- Secondary Outcome Measures
Name Time Method 1.Maternal pyrexia<br>2.Neonatal pyrexia<br>3.Prelabour rupture of membranes<br>4.Mode of delivery - whether successful vaginal delivery, instrumental vaginal delivery or caesarean delivery<br>5. Percentage of spontaneous onset of labour (SOL) in women in all three groups.<br> <br>6. Percentage of women who required the vaginal PGE2 a<br> <br><br> [1.First ten days post partum<br>2.Until discharge<br>3. Till spontaneous onset of labour<br>4. Delivery<br>5.Between 40 week + 4 days to 40 week+6 days<br>6. At 40 weeks and 6 days]<br>