Arthroscopic rotator cuff repair: Trans-osseous versus anchor technique
Phase 1
Completed
- Conditions
- Musculoskeletal Diseases
- Registration Number
- PACTR202404475835971
- Lead Sponsor
- Menoufia University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Rotator cuff tear
MRI evidence of tear
at least three months of symptoms duration
inadequate response to conservative measures
Exclusion Criteria
patients with massive rotator cuff tears
irreparable tears
frozen shoulder
inflammatory or rheumatologic diseases
glenohumeral osteoarthritis
previous shoulder surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms underlying trans-osseous rotator cuff repair compared to anchor techniques?
How does trans-osseous technique compare to anchor-based repair in terms of clinical outcomes for rotator cuff tears?
Are there specific biomarkers that predict successful healing outcomes in trans-osseous versus anchor rotator cuff repair methods?
What are the potential adverse events associated with arthroscopic trans-osseous rotator cuff repair techniques?
How does the trans-osseous technique for rotator cuff repair compare with other surgical approaches in musculoskeletal disease management?