Prospective randomized controlled evaluation of the outcomes of two different postoperative therapeutic concepts for rotator cuff repair surgery
Not Applicable
- Conditions
- M75.1Rotator cuff syndrome
- Registration Number
- DRKS00017519
- Lead Sponsor
- Klinische StudieneinheitOrthopädische Klinik, Universität Würzburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 74
Inclusion Criteria
Patients with rotator cuff repair surgery
Exclusion Criteria
Not eligible for surgery
Revision-Surgery
Server osteoarthritis
Preoperative frozen shoulder
massive tear (> 5cm)
wide tendon retraction
massive atrophy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method prevalence of reruptures 1 year postop
- Secondary Outcome Measures
Name Time Method Range of motion, life quality, strength in the operated shoulder, pain level