Comparison of pain, pain medicine requirement and in patients undergoing spine surgeries.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/09/036430
- Lead Sponsor
- Department Of Neuroanaesthesia and Neurocritical care NIMHANS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age â?? 18 to 65 years,
Either gender,
ASA grade I to III,
Elective spine surgeries in prone position involving up to 4 vertebral levels and lasting up to 6 hours
Exclusion Criteria
Surgeries involving C1 and C2 levels,
Spine tumors requiring TIVA and neuromonitoring,
Any contraindications to regional block such as local infections or allergy to local anesthetics,
Refusal of consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the intraoperative opioid consumption and acute postoperative pain (up to 48hours) in patients undergoing spine surgeries with and without ESP blockTimepoint: 48hours
- Secondary Outcome Measures
Name Time Method