Comparison of pain relief using block technique with intravenous analgesia technique in lumbosacral spine surgeries
Phase 1
- Conditions
- Health Condition 1: M511- Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathyHealth Condition 2: M511- Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy
- Registration Number
- CTRI/2023/07/055221
- Lead Sponsor
- AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Patients undergoing elective lumbo-sacral spine
surgeries.
2) ASA grade I + II + III
3) Age 18 years to 70 years.
Exclusion Criteria
1) Patient refusal to participate in the study
2) Known hypersensitivity to local anaesthetic and
opioids.
3) Infection at the site of block.
4) Anticoagulation therapy.
5) Bleeding diathesis and coagulopathies.
6) Pregnancy.
7) Unable to understand numerical rating scale (NRS) for pain assessment and function of patient-controlled analgesia (PCA) pump
8) History of renal, hepatic, cardiac and neurological diseases
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total postoperative fentanyl requirement at 24hoursTimepoint: At the end of 24 hours
- Secondary Outcome Measures
Name Time Method