Comparison of pain relief in patients undergoing spine surgery between Buprenorphine patch and Intravenous Tramadol
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified
- Registration Number
- CTRI/2023/06/053532
- Lead Sponsor
- VMMC AND SAFDARJUNG HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients aged 18-60 years belonging to American society of anaesthesiology physical status (ASA) grade I & II undergoing elective spinal surgery.
Exclusion Criteria
Any known history of allergy to buprenorphine, pregnancy and lactation, Patients on antidepressants, on opioid therapy, opioid dependant or sensitive
patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess Total dose of rescue analgesics requiredTimepoint: 24hr, 48hr post surgery
- Secondary Outcome Measures
Name Time Method To assess: <br/ ><br>VAS score <br/ ><br>Hemodynamic parameters: Heart rate, systolic, diastolic and mean arterial Pressure <br/ ><br>Time of first rescue analgesic requirementTimepoint: 30min, 2hr, 4hr, 6hr, 12hr, 24hr