Pain in patients undergoing shoulder surgery using interscalene in comparison with anterior suprascapular nerve block technique
Phase 2
Recruiting
- Conditions
- Patients undergoing shoulder surgery.
- Registration Number
- IRCT20220425054655N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients undergoing atherosclerotic shoulder surgery,
People 21 years and older,
body mass index 18-35 kg / m2
Complete satisfaction from participating in the study
Exclusion Criteria
Patients who are unable to express satisfaction
People who have been chronically treated for opioids
People who are allergic to the drugs under study
People with neurological defects
Patients with advanced lung disease (COPD and uncontrolled asthma)
Surgeries over 3 hours
People who have any contraindications to local anesthesia such as coagulopathy and local infection
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain scoring. Timepoint: 16 and 24 hours after surgery. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method