TRIAL FOR USE OF LOCAL ANAESTHETIC AGENT IN LAPAROSCOPIC GYNAECOLOGICAL SURGERIES FOR REDUCING POST OPERATIVE PAI
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: null- all patients undergoing gynaecological operative procedures
- Registration Number
- CTRI/2017/05/008664
- Lead Sponsor
- Armed Forces Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
ASA status I & II
All cases of Operative laparoscopic gynaecological surgeries
Exclusion Criteria
Laparoscopic Gynaecological Oncology surgeries
history of opiod use/ alcohol abuse in last 24 hours prior to study
Weight < 50kg
history of allergy to the drug in study
Chronic Pain Syndrome
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To evaluate the efficacy of port site and intraperitoneal Bupivacaine in reducing post operative pain by comparing VAS scores between intervention and control armTimepoint: 2 hour, 4hours and 8 hours post operatively
- Secondary Outcome Measures
Name Time Method 1.To evaluate the safety and note the side effects if any of port site and intraperitoneal Bupivacaine used for reducing post operative pain <br/ ><br> <br/ ><br>2.To compare the need for rescue analgesia between the intervention and control armTimepoint: 2 hour, 4hours and 8 hours post operatively