Operative Therapy of Acromioclavicular Joint SeperationsMedium- and longterm results after operative therapy of Acromioclavicular Joint Dislocations with a hookplate
Recruiting
- Conditions
- S43.1Dislocation of acromioclavicular joint
- Registration Number
- DRKS00009446
- Lead Sponsor
- Berufsgenossenschaftliche Unfallklinik Tübingen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
operative therapy of an AC-Luxation with a hookplate at the BGU Tübingen
Exclusion Criteria
patient does not want to participate
patient cannot be examined or interviewed
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is to assess the functional outcome of the applied therapy. The Trial includes an extended clinical examination and consultation of the patients. This will be done in the context of a regular consultation-hour. The data is to be assesed according to the DASH-Score (Disability of arm, shoulder and hand), the Constant Score, the SF-36 Score (which assesses the patients subjective perception in everyday situations and the patients experiences of pain or lack thereof), the Visual Analog Scale (VAS) and a survey created for this study that gathers various parameters. The Primary Outcome is planned with first examination date of at least one year after completing the therapy.
- Secondary Outcome Measures
Name Time Method ongterm effects and complications (Survey). The point of time for the secondary outcome is set for 5 years after completing the therapy.