Comparison of three methods of pain relief in patients undergoing gall bladder surgery
Phase 4
- Conditions
- Health Condition 1: null- patients scheduled to undergo laparoscopic cholecystectomy
- Registration Number
- CTRI/2013/03/003493
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
•ASA physical status I-II
•Age 18-65 yrs
•Body weight 50-75 kg of either sex ( BMI - >18.5 to <25 )
Exclusion Criteria
•History of relevant drug allergy
•Age 18yrs or 65yrs
•History of psychiatric illness , substance abuse , or medical therapies resulting in tolerance to opioids
•Acute cholecystitis or pancreatitis
•Severe cardiovascular , respiratory ,metabolic or neurological disease
•Surgery requiring postoperative intra-abdominal drainage
•Pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare and evaluate post operative pain scores after administration of US guided TAP block, port site infiltration and intraperitoneal instillation with ropivacaine in laparoscopic cholecystectomy.Timepoint: To compare and evaluate post operative pain scores after administration of US guided TAP block, port site infiltration and intraperitoneal instillation with ropivacaine in laparoscopic cholecystectomy in the immediate post operative period and then at 10 min, 30 min, 60 min, 4 hours, 8 hrs, 12 hrs and 24 hrs.
- Secondary Outcome Measures
Name Time Method 1.To compare and evaluate post operative nausea and vomiting scores. <br/ ><br>2. To calculate the total amount of rescue analgesic used in all the patients. <br/ ><br>3. To note any side effect due to the technique or the drug used for the post operative pain relief. <br/ ><br>Timepoint: Post operative period upto 24 hrs