Study comparing the efficacy of intravenous oxytocin and intravenous carbetocin in haemodynamic stability of patients undergoing caesarean section under spinal anesthesia
Phase 3
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2022/08/044710
- Lead Sponsor
- Sabari C G S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Age between 18 to 40 years.
2)American Society of Anaesthesiologists physical status II
3)Patients undergoing elective caesarean section under regional anaesthesia.
4)Provides Consent.
Exclusion Criteria
1)Presence of hypertension, preeclampsia, cardiac, renal or liver diseases, epilepsy and patients undergoing general anaesthesia.
2)Patient who are unable or unwilling to give consent.
�Women with history of hypersensitivity to carbetocin.
�Patients who do not fulfil inclusion criteria.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to compare the haemodynamic effects of oxytocin and carbetocinTimepoint: 15 seconds before giving drug <br/ ><br>every 15 seconds for 5 minutes after giving drug
- Secondary Outcome Measures
Name Time Method use of additional uterotonic agents <br/ ><br>haemoglobin level preoperatively andTimepoint: 2 hours and 24 hours postoperatively