Comparison of different doses of Oxytocin during caesarian delivery
Not Applicable
- Registration Number
- CTRI/2023/07/054979
- Lead Sponsor
- medical Superintendent
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)ASA PS I and II
2)Aged between 18 to 40 years
3)Elective Cesarean section under Spinal anaesthesia
Exclusion Criteria
1.Previous history of oxytocin allergy
2.Valvular diseases complicating pregnancy
3.Other cardiac diseases complicating pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of efficacy & safety of two different doses of Oxytocin during caesarean deliveryTimepoint: 4
- Secondary Outcome Measures
Name Time Method Adequacy of uterine contractions <br/ ><br>Haemodynamic changes <br/ ><br>3.Requirement of additional uterotonic agents. <br/ ><br>4.Adverse effectsObjectives: To compare the following parameters between two different doses of oxytocin <br/ ><br>Timepoint: 4