CTRI/2022/08/044710
Not yet recruiting
Phase 3
A Randomised control trial comparing the efficacy of intravenous oxytocin and intravenous carbestocin in haemodynamic stability of patients undergoing caesarean section under spinal anesthesia
Sabari C G S0 sites0 target enrollmentTBD
ConditionsHealth Condition 1: 1- Obstetrics
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: 1- Obstetrics
- Sponsor
- Sabari C G S
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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.
- •ââ?¬Â¢Women with history of hypersensitivity to carbetocin.
- •ââ?¬Â¢Patients who do not fulfil inclusion criteria.
Outcomes
Primary Outcomes
Not specified
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