A clinical trial to study recommendation based and the effects of local infiltration in patients undergoing laparoscopic cholecystectomy.
Phase 4
- Conditions
- Health Condition 1: null- All patients ASA Physical status 1and 2 For laproscopic cholecystectomy.
- Registration Number
- CTRI/2015/10/006248
- Lead Sponsor
- nil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 54
Inclusion Criteria
ASA I â?? II
Laparoscopic cholecystectomy using 3-4 ports
Exclusion Criteria
Patients refusal
Emergency surgery
H/o allergic reactionto local anaesthestic drugs
Pregnancy and lactating mothers
Requiring more than 3 doses of rescue analgesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS score for post operative pain <br/ ><br>Immediate post extubation,Timepoint: 1, 2, 4, 6, 12, 24 hours postoperative
- Secondary Outcome Measures
Name Time Method umber of analgesi demands, pulse, MAP, SpO2Timepoint: 1, 2, 4, 6, 12, 24 hours postoperative