Study to assess the analgesic effect of two different methods in patients undergoing laparoscopic removal of gallbladder surgeries.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/03/051022
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All ASA grade I and grade II patients between 20-60 years age group
Exclusion Criteria
· All ASA grade III and IV patients.
· Diabetes and Hypertension.
· Cardiovascular, respiratory and neurological disorders.
· Obesity (BMI >30kg/m2)
. Drug allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time for first request of analgesia postoperatively is noted which gives the duration of analgesia <br/ ><br>Postoperative visual Analogue score scale at various time intervals <br/ ><br> <br/ ><br> <br/ ><br>Timepoint: Immediately after surgery,1st hour,2nd hour,4th hour,6th hour,8th hour,12th hour,16th hour,20th hour,24th hour
- Secondary Outcome Measures
Name Time Method Adverse effects such as nausea,vomiting,sedation,respiratory depression, shoulder pain,shivering assessed postoperatively at various time intervalsTimepoint: Immediately after surgery,1st hour,2nd hour,4th hour,6th hour,8th hour,12th hour,16th hour,20th hour,24th hour