CTRI/2024/07/070090
Not yet recruiting
Phase 4
A randomised clinical study to compare time to post-operative recovery using propofol with either ketamine or dexmedetomidine by target control infusion in patients undergoing laparoscopic cholecystectomy - nil
ady hardinge medical college0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- ady hardinge medical college
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients of either sex in the age group of 18\-65 yrs.
- •2\.ASA I and ASA II.
- •3\.Patients undergoing laparoscopic cholecystectomy.
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Not specified
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