1.To determine the difference in VAS score between both the groups.2.To determine the difference in time for need of first rescue analgesia and total number of doses of rescue analgesic required during first 72 hours postoperatively between both the groups.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/09/036226
- Lead Sponsor
- Sawai Man Singh Medical College And Attached Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients undergoing aorto-femoral graft surgery
2.Patient willing to give written informed consent
3.Patient of either sex
4.Weighing 40 to 70 kg â??BMI <40kg/m2
Exclusion Criteria
1.Patient refusal
2.known or admitted alcohol or drug abusers
3.Allergic to drugs involved in study
4.Patient taking any drug that have interaction with tramadol and Buprenorphine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.To determine the difference in VAS score between both the groups. <br/ ><br>2.To determine the difference in time for need of first rescue analgesia and total number of doses of rescue analgesic required during first 72 hours postoperatively between both the groups. <br/ ><br>Timepoint: 72 hours
- Secondary Outcome Measures
Name Time Method 1.To determine the difference in sedation score in both the groups <br/ ><br>2.To assess and compare Hemodynamic parameters: (Heart Rate; Mean Blood Pressure; Systolic Blood Pressure; Diastolic Blood Pressure),. <br/ ><br>3.To determine the difference in percentage of cases who develop side effects ( if any)in both groups in first 72 hours <br/ ><br>Timepoint: 72 hours