A comparative study of pain management techniques for surgeries of the backbone
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/02/062635
- Lead Sponsor
- Manipal Hospital Whitefield
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anaesthesiologists physical status 1 - 3
Exclusion Criteria
Patients who are allergic to local anaesthetics.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 24-hour postoperative pain scores using Numeric Rating Scare (NRS 0 - 10)Timepoint: Baseline (0 hour in the postoperative period); 2 hours; 4 hours; 8 hours; 12 hours, 24 hours in the postoperative period
- Secondary Outcome Measures
Name Time Method To compare the number of rescue analgesics needed between patients receiving and not receiving Erector spinae plane block for elective lumbar spine surgery under general anaesthesia.Timepoint: 24 hours after surgery;To compare the patients pain control satisfaction between patients receiving and not receiving Erector spinae plane block for elective lumbar spine surgery under general anaesthesia.Timepoint: 24 hours after surgery