â??A study to compare efficacy of two types of pain relief methods i.e injection at the operation site in the skin versus putting the medicine in the abdominal cavity combined with injection at operation post operative pain relief and effect on recovery after laproscopic cholecystectomyâ??
Not Applicable
Completed
- Conditions
- Health Condition 1: null- good
- Registration Number
- CTRI/2017/09/009875
- Lead Sponsor
- dr sanjeevani zadkar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1.ASA I-II patients
2.patients undergoing Laparoscopic cholecystectomy using 3-4 ports
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary objective <br/ ><br>1.post operative pain score using VISUAL ANALOGUE SCALE till 48 hrs <br/ ><br>Timepoint: Primary objective <br/ ><br>1.post operative pain score using VISUAL ANALOGUE SCALE till 48 hrs <br/ ><br>Secondary outcomes <br/ ><br>1.time taken for recovery to normal activity &walking around without support <br/ ><br>2.feeling of wellbeing on ordinal scale 1-5 for first 5 days postoperatively <br/ ><br>3. rescue analgesia requirement-no of doses and timings <br/ ><br>4.duration of stay in recovery room in minutes <br/ ><br>5.incidence of nausea and vomitting-in form of present or absent <br/ ><br>
- Secondary Outcome Measures
Name Time Method Secondary outcomes <br/ ><br>1.time taken for recovery to normal activity &walking around without support <br/ ><br>2.feeling of wellbeing on ordinal scale 1-5 for first 5 days postoperatively <br/ ><br>3. rescue analgesia requirement-no of doses and timings <br/ ><br>4.duration of stay in recovery room in minutes <br/ ><br>5.incidence of nausea and vomitting-in form of present or absent <br/ ><br>Timepoint: till 5 days post op