Erector spina block in lumbar spinal surgery
Phase 3
Recruiting
- Conditions
- Pain control after spinal surgery.Other acute postprocedural painG89.18
- Registration Number
- IRCT20200628047936N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
All candidated 18-75 y/o patients for spinal lumbar surgery
patients with normal hepatic and renal function
ASA score 1-2
Exclusion Criteria
addiction
BMI more than 35 or less than 16
allergy to local anesthetics
mental disorders
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postop pain score in defined intervals. Timepoint: 1, 2 , 4, 6, 12, 24 Hours after surgery. Method of measurement: Pain scale chart (NRS).;Opioid consumption in first postop 24 hours. Timepoint: First 24 hours. Method of measurement: Amount of Opioid consumption recorded by nurse.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the analgesic effects of erector spina block in post-lumbar surgery pain management?
How does ultrasound guided erector spina block compare to traditional epidural analgesia for postoperative pain in lumbar spinal surgeries?
Are there specific biomarkers that predict optimal response to erector spina block in patients undergoing lumbar spinal procedures?
What are the potential adverse events associated with ultrasound guided erector spina block in spinal surgery patients and how are they managed?
What combination analgesic strategies are being explored alongside erector spina block for enhanced postoperative pain control in lumbar spinal surgery?