Health Condition 1: O668- Other specified obstructed labor
Conditions
Interventions
Intervention1: Its RANDOMISED CONTROL TRIAL
MISOPROSTOL tablet in form of solution (200microgram tablet in 200 ml water is dissolved and every 2 hourly 20ml of solution used for labor induction instea
Sponsors
Room No Unit II king george medical college queen Mary hospital
Eligibility
Inclusion criteria
Inclusion criteria: Singleton live pregnancy, 34 weeks gestation, Bishop score more than 6, Intact membranes, Cephalic presentation, Reassuring fetal heart rate Patients giving written informed consent will be taken
Exclusion criteria
Exclusion criteria: Hypersensitivity to misoprostol, Previous cesarean delivery or other uterine surgery, Uterine contractions, and Significant maternal cardiac, renal, or liver disease. Not giving consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Induction delivery interval and rate of lower segment cesarean section (LSCS) Timepoint: Outcome will be assessed between 24-48 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the effectiveness, safety profile, & impact on maternal & neonatal outcomes.Timepoint: from induction to delivery of baby up to 48hours Mode of delivery Any uterine hyper stimulation Feral heart rate abnormalities Medium stained liquor Nice admission morbidity/mortality | — |
Countries
India
Contacts
Public ContactDr Manju Lata Verma
King Georges Medical University Lucknow
Outcome results
None listed