ong term results of arthroscopic debridement of partial rotator cuff ruptures.
Withdrawn
- Conditions
- partial rotator cuff rupture10005944
- Registration Number
- NL-OMON41074
- Lead Sponsor
- Onze Lieve Vrouwe Gasthuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
All patients diagnosed with a partial rotator cuff rupture, confirmed by MRI or ultrasound
All patients who received arthroscopic debridement at the department of orthopaedic surgery of the OLVG between January 2001 and December 2004;
Patients older than 18 years at the moment of diagnosis partial rotator cuff rupture;
Surgical intervention: debridement with or without acromioplasty
Exclusion Criteria
Inadequate knowledge of Dutch language;
Post-operative incident of ipsilateral shoulder injury such as fractures or AC separation or shoulder dislocation;
Neurological conditions influencing upper limb;
Unable to visit the outpatient clinic to undergo CMS testing;
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Long term results (minimum 10 years) of arthroscopic debridement of partial<br /><br>rotator cuff ruptures as measured with the CMS. </p><br>
- Secondary Outcome Measures
Name Time Method <p>n.a.</p><br>