Randomized double blind placebo controlled study of outpatient misoprostol for term pregnant patientswith no risk factors to prevent routine induction of labour and to prevent post dated pregnancy and its complications
Phase 3
Completed
- Conditions
- Health Condition 1: null- PREGNANCY
- Registration Number
- CTRI/2013/08/003883
- Lead Sponsor
- CMCH AND HOSPITAL VELLOREHRISTIAN MEDICAL CO
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 126
Inclusion Criteria
SINGLETON PREGNANCY AT 38+4WEEKS TO 39+4WEEKS GESTATION,CEPHALIC PRESENTATION,BISHOP SCORE LESS THAN 4,LACK OF CURRENT INDICATION FOR INDUCTION OF LABOUR
Exclusion Criteria
RUPTURE OF MEMBRANES,UNEXPLAINED VAGINAL BLEEDING,PRIOR UTERINE INCISION,GESTATIONAL HYPERTENSION,GESTATIONAL DIABETES ,ESTIMATED FETAL WEIGHT MORE THAN 4500GMS
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method INTERVENTION TO DELIVERY INTERVALTimepoint: DURING DELIVERY
- Secondary Outcome Measures
Name Time Method Gestational age at delivery,spontaneous onset of labour or induction of labour,LSCS for failed induction,meconium aspiration syndrome,APGAR less than 6 at 5minutes,NICU admissions,rupture of membranes,bleeding per vaginmTimepoint: same