This study assesses the amount of pain relief needed by patients undergoing lumbar spine surgeries after receiving either an Ultrasound Guided TLIP Block or an Ultrasound Guided Lumbar ESP Block.
Phase 2
- Conditions
- Health Condition 1: M488- Other specified spondylopathies
- Registration Number
- CTRI/2023/11/060131
- Lead Sponsor
- DEPT OF ANAESTHESIOLOGY AND CRITICAL CARE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age between 18 and 65 years
2. ASA grade 1 to 2
3. patients scheduled for single level non traumatic lumbar spinal surgeries.
Exclusion Criteria
1. Patient refusal
2. Age below 18 or above 65 years.
3. ASA grade III to IV
4. Patients with known allergies to any of the drugs used.
5. History of chronic opioid consumption
6. Coagulation disorder
• Cognitive disorder (major depression or generalized anxiety
disorder)
• Infection at the injection site
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total NSAIDS requirements [ Time Frame: 24 hours <br/ ><br>postoperatively] <br/ ><br> <br/ ><br>Amount of NSAIDS required postoperatively. <br/ ><br>Timepoint: Amount of NSAIDS required at 2, 4, 6, 12, 18, and 24hours immediate postoperatively. <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1. Visual analogue pain score [ Time Frame: at rest at 2, 4, 6, 12, 18, and 24hours postoperatively] <br/ ><br> <br/ ><br>2. Time to first postoperative analgesic request [ Time Frame: 24 hours postoperatively] <br/ ><br> <br/ ><br> <br/ ><br>3.To estimate the incidence of motor block among both the groups [ Time Frame: at 6, 12 and 24 hourspostoperatively]Timepoint: 24 hours postoperatively <br/ ><br>