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Clinical Trials/CTRI/2022/08/044710
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

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional

Investigators

Sponsor
Sabari C G S

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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