Brachial plexus block compared with periarticular injection for pain control following arthroscopic rotator cuff repair: a randomized controlled trial
Not Applicable
- Conditions
- Rotator cuff tear
- Registration Number
- JPRN-UMIN000015684
- Lead Sponsor
- St. Luke's international hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 34
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with ASA status III-V, renal insufficiency, hepatic insufficiency, blood coagulation abnormality, prolonged QT interval on electrocardiograms, respiratory complication, poor controlled DM, and allergy or intolerance to one of the study drugs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method