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Clinical Trials/CTRI/2024/07/071613
CTRI/2024/07/071613
Not yet recruiting
Phase 3

A RANDOMISED COMPARATIVE STUDY FOR CARDIACPRECONDITIONING EFFECT OF KETAMINE-DEXMEDETOMIDINEVERSUS FENTANYL-PROPOFOL IN PATIENTS UNDERGOING CARDIACSURGERY IN THE DEPARTMENT OF ANAESTHESIA. - NI

SMS Medical College and Hospital0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: O- Medical and Surgical

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
SMS Medical College and Hospital
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
SMS Medical College and Hospital

Eligibility Criteria

Inclusion Criteria

  • •1\. Informed written consent for the study
  • •2\. All patients will be American Society of Anaesthesiologists physical status II\-III.
  • •3\. Aged between 18 and 70 years.
  • •4\. Weight between 40 and 70 kg.
  • •5\. BMI less than 30\.
  • •6\. New York Heart Association classification of cardiac function II\-III,
  • •7\. Ejection fraction greater than 40%

Exclusion Criteria

  • •1\. Patient should not part of any other study.
  • •2\. Non cooperative patient.
  • •3\. Patient with history of acute myocardial infarction.
  • •4\. Elevated levels of circulating cardiac troponin
  • •5\. History of endocrine, metabolic, neurological and psychotic disorder
  • •6\. History of previous unusual response to ketamine, dexmedotomidine, fentanyl,

Outcomes

Primary Outcomes

Not specified

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