Evaluation of the effectiveness of pain relief by Thoracolumbar interfascial plane block in patients undergoing spinal surgeries
Not Applicable
- Conditions
- Health Condition 1: G959- Disease of spinal cord, unspecifiedHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2021/03/031682
- Lead Sponsor
- Department of anaesthesia and intensive care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade 1 and 2 scheduled to undergo elective spinal surgeries
Exclusion Criteria
History of allergy to local anaesthesia
Contraindications to the block(coagulaopathies,anticoagulants)
Inability to understand pain scale
Inability to PCA pump
Body mass index >30
Previous lumbar spinal surgeries
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the efficacy of the ultrasound guided thoracolumbar interfascial plane block in patients undergoing lumbar spinal surgeriesTimepoint: at baseline,2,4,6,12,24 and 48 hours of surgery
- Secondary Outcome Measures
Name Time Method To assess the following parameters in adult patients undergoing lumbar spinal surgeries in both the groups <br/ ><br>1.to compare the time to first analgesic in each group <br/ ><br>To compare the total morphine consumption over 24 hrs in both the groups <br/ ><br>To compare the patient satisfaction in terms of quality of pain relief using the likert scaleTimepoint: At 0,2,4,6,8,10,12,24 hrs of surgery