The effect of spinae plane block and retrolaminar block on pain control
Phase 3
- Conditions
- Pain.Pain, not elsewhere classified
- Registration Number
- IRCT20120814010599N28
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Patients' consent to enter the study
Patients with ASA <1 & 2
Patients aged 20-60 years
Patients undergoing upper abdominal laparoscopic surgery
Exclusion Criteria
Emergency patients
History of ropiavacaine allergy
Patients who have received analgesia in a recent day
Patients with a Body Mass Index>35
Patients with or underlying liver and kidney disease and coagulopathy
Patients addicted to opioids
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: After the end of surgery and 20 minutes, 2 hours, 4 hours, 6 hours, 12 hours and 24 hours after surgery. Method of measurement: Using Numeric Rating Scale (NRS).
- Secondary Outcome Measures
Name Time Method Patient satisfaction. Timepoint: After the end of surgery and twenty minutes, 2 hours, 4 hours, 6 hours, 12 hours and 24 hours after surgery. Method of measurement: poor:0,moderate:1,good:2,very good:3,excellent:4.