To study the effect of clonidine on dose reduction of propofol in patients undergoing laparoscopic cholecystectomy
Not Applicable
- Conditions
- Health Condition 1: K801- Calculus of gallbladder with othercholecystitis
- Registration Number
- CTRI/2020/06/026034
- Lead Sponsor
- Department of Anesthesiology rd floor PGIMER building ABVIMS and Dr RML Hospital New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients with ASA Grade 1 & 2
2.Posted for Laparoscopic surgery
Exclusion Criteria
1.Pregnancy
2.BMI >35kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.PRST Score-It will be less than 2 <br/ ><br>2.By seeing Bispectral indexTimepoint: 1-2 hours during intraoperative period
- Secondary Outcome Measures
Name Time Method 1.Intraoperative hemodynamics monitoring-HR,MAP <br/ ><br>2.For extubation-Time to reach BIS more than 80 after stopping propofol infusionTimepoint: At baseline untill surgery completed