The efficacy of the concomitant use of continuous interscalene block and suprascapular nerve block for pain relief after arthroscopic rotator cuff repair
Not Applicable
- Conditions
- rotator cuff tear
- Registration Number
- JPRN-UMIN000027291
- Lead Sponsor
- yamagata university faculty of medicine department of anesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
When we did not obtain written informed consent, we failed the continuous interscalene block or the suprascapular nerve block, a patient had a contraindication of the nerve blocks, a patient could not perform self-evaluation or communicate with us such as a mental illness, or a patient had a severe underlying condition
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain at 6 hours, 12 hours, 24 hours, 48 hours after the operation: Numerical Rating Scale (0-10), Verbal Rating Scale (0-3)
- Secondary Outcome Measures
Name Time Method The amount of additional analgesics, complications and adverse effects during 48 hours after the operation.