Comparing the effects of bupivacaine and bupivacaine-methylprednisolone in ultrasound guided erector spinae plane block on postoerative pain in Lumbar spine surgery
Phase 3
Recruiting
- Conditions
- umbar discopathy.Other intervertebral disc degeneration, lumbar regionM51.36
- Registration Number
- IRCT20210415050983N6
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 64
Inclusion Criteria
Patients 18-65 years old are candidates for two or three level spine surgery
ASA score 1-2
Normal kidney and liver function
Patient consent to perform the block
No history of allergies to local anesthetics
No drug addiction
No diabetes
Exclusion Criteria
Increase the scope of surgery to more than three level
Extending the length of surgery for more than 6 hours
Block site infection or systemic
History of anticoagulant use
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraoperative isoflurane Consumption in tow groups. Timepoint: Before the start of anesthesia and after the end of anesthesia. Method of measurement: By a graduated glass based on mL.;Intraoperative fentanyl consumption in the two groups. Timepoint: End of surgery. Method of measurement: Dosage consumed based on mcg.;Pain after surgery. Timepoint: 0, 1 and 6 hours after surgery and one month after surgery. Method of measurement: NRS.;Blood sugar. Timepoint: After surgery up to 24 months. Method of measurement: Blood test.
- Secondary Outcome Measures
Name Time Method ausea and vomiting. Timepoint: 0, 1 and 6 hours after surgery. Method of measurement: Ask the patient.