To compare the pain score after operation in patients undergoing laminectomy surgeries by spraying buprenorphine and saline in epidural space
Phase 3
- Conditions
- Health Condition 1: G952- Other and unspecified cord compression
- Registration Number
- CTRI/2024/03/063857
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients willing to give informed and written consent
ASA physical status I & II
Patients with body weight 50-80kgs
Exclusion Criteria
ASA physical status III and above.
Patients who have known hypersensitivity to the study drugs
Patients with history of neuromuscular disease
Patients with history of substance abuse
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain by Numerical pain rating scale <br/ ><br>Timepoint: 1st, 2nd, 3rd, 4th, 5th, 6th, 12th, 18th and 24 hours
- Secondary Outcome Measures
Name Time Method Pulse Rate <br/ ><br>Mean Arterial Pressure <br/ ><br>Respiratory Rate <br/ ><br>SpO2 <br/ ><br>Timepoint: 1st, 2nd, 3rd, 4th, 5th, 6th, 12th, 18th and 24 hours