comparison of changes in blood pressure following supplementation of either of the two drugs named oxytocin and carbetocin in surgeries done in pregnant mothers following the delivery of the baby.
Phase 3
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2024/05/067030
- Lead Sponsor
- oorul Aashika A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Parturient acceptance
2.ASA status 2 and 3
3.Age between 20-30 yrs.
4.Parturient of term gestation undergoing elective lower segment cesarean section under spinal anesthesia
Exclusion Criteria
1.Absolute contraindications for spinal anesthesia
2.Combined spinal epidural anesthesia
3.Short stature <145cm and BMI > 40
4.Conditions associated with increased level of PPH risk (placenta previa, placentalabruption, multiple gestation)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary objective of this study is to compare the mean arterial blood pressure variation following administration of oxytocin and carbetocin in lower segment cesarean section.Timepoint: Baseline, 1,3,5,10 minutes and every 2nd minute following delivery of baby till 20 minutes
- Secondary Outcome Measures
Name Time Method The secondary objective focusses on <br/ ><br>1.Heart rate variations occurring between oxytocin and carbetocin <br/ ><br>2.Requirement of vasopressor - phenylephrine <br/ ><br>3.Clinical estimation of blood loss <br/ ><br>4.Side effects and complications of oxytocin and carbetocin <br/ ><br>Timepoint: Baseline, 1,3,5,10 minutes and every 2nd minute following delivery of baby till 20 minutes