A study to compare pain relief with erector spinae plane block (local anaesthetic injected below erector spinae muscle on the back) and patient controlled analgesia ( self-control device) after spine surgery.
Not Applicable
Completed
- Conditions
- Health Condition 1: G544- Lumbosacral root disorders, not elsewhere classified
- Registration Number
- CTRI/2020/01/023068
- Lead Sponsor
- AIIMS Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 54
Inclusion Criteria
Patients belonging to ASA physical status I or II and scheduled for elective thoracic/lumbar spine surgery will be enrolled.
Exclusion Criteria
Patients who refused to participate, pregnant female, patient with baseline cognitive deficits sufficient to make objective pain assessment unreliable, coagulopathy, liver and renal dysfunction, preoperative neurological deficits and allergy to amide local anaesthetics or opioid will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method