SE OF OXYTOCIN DURING EMERGENCY CESAREAN SECTION: A STUDY COMPARING OXYTOCIN INFUSION WITH & WITHOUT OXYTOCIN BOLUS
Not Applicable
- Conditions
- Health Condition 1: null- women for emergency cesarean section
- Registration Number
- CTRI/2013/12/004193
- Lead Sponsor
- Dr RPGMC Kangra at Tanda HP
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
•Singleton pregnancy/Woman for emergency caesarean section as per obstetrical indication/Period of gestation between 36 to 41 weeks
Exclusion Criteria
•Twin pregnancy /severe pre-eclampsia/ HELLP syndrome/Co-agulopathy/Abruptio placentae/Intra-uterine fetal death/Malformed fetus/Uncontrolled diabetes mellitus/Chorio-amniotis/Known case of thrombophilia/ Known case of chronic Renal or liver disease /previous classical caesarean section/ hysterotomy/previous uterine surgery (caesarean section, myomectomy, hysterotomy, polypectomy, lysis of uterine synechia, or hysteroscopic metroplasty)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method PRIMARY OUTCOME <br/ ><br>The primary outcome is major obstetrical hemorrhage following caesarean section. (defined as blood loss 1000ml ). <br/ ><br>Timepoint: 24 hours after LSCS
- Secondary Outcome Measures
Name Time Method â?¢Hemodynamic profile ( BP, mean arterial pressure, pulse rate) <br/ ><br>â?¢Severe anemia ( 20% fall in Hb post operative) <br/ ><br>â?¢Need of blood transfusion <br/ ><br>â?¢Side effect profile <br/ ><br>â?¢Duration of surgery <br/ ><br>â?¢Need for manual removal of placenta <br/ ><br>Timepoint: 24 hours after LSCS