CTRI/2013/12/004193
Not yet recruiting
未知
A randomized control trial comparing use of oxytocin bolus with and without oxytocin infusion in women with cesarean section after extraction of fetus
Dr RPGMC Kangra at Tanda HP0 sites80 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- women for emergency cesarean section
- Sponsor
- Dr RPGMC Kangra at Tanda HP
- Enrollment
- 80
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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)
Outcomes
Primary Outcomes
Not specified
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