Study to compare post operative recovery time with propofol plus ketamine vs propofol plus Dexmedetomidine by target control infusion in patients undergoing laparoscopic cholecystectomy
Phase 4
Not yet recruiting
- Conditions
- Health Condition 1: K80-K87- Disorders of gallbladder, biliary tract and pancreas
- Registration Number
- CTRI/2024/07/070090
- Lead Sponsor
- ady hardinge medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method