The efficacy and safety of the arthroscopic lateral acromioplasty along with arthroscopic rotator cuff repair
Not Applicable
- Conditions
- rotator cuff tear
- Registration Number
- JPRN-UMIN000041432
- Lead Sponsor
- Yokohama City University Medical Center, Department of Orthopedic Surgery
- 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
(1) The patients during pregnancy, with possibility of pregnant and hoping pregnant during investigation period of this study. (2) The patients can not be performed MRI (3) The past history of trauma or operation on the ipsilateral shoulder (4) The patients who were affected in inflammatory disease. (5) Rotator cuff tear arthropathy of more than or equal grade 4 on Hamada classification (6) Os acromiale
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Retear rate on magnetic resonance imaging 6 months postoperatively
- Secondary Outcome Measures
Name Time Method