Clinical, structural and functional outcome after pediatric injury of anterior cruciate ligament
Recruiting
- Conditions
- S83.53M23.51S82.18
- Registration Number
- DRKS00031396
- Lead Sponsor
- BG Klinikum Duisburg gGmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Rupture of the anterior cruciate ligament with ACL reconstruction by means of hamstring tendon autograft or intercondylar eminence avulsion fractures of ACL with eminence fracture fixation
Exclusion Criteria
•Multiligament injuries requiring medical treatment
•Contralateral injuries requiring medical treatment
•Missing Declaration of consent and rejection of study-participation by patient, parent or legal guardian
•Patients who are not able to consent
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment and investigation of the relationship between subjective treatment outcome at least 24 month after the cruciate ligament surgery using the IKDC 2000 score and clinical, radiological (MRI) as well as biomechanical parameters.
- Secondary Outcome Measures
Name Time Method - Assessment of knee function and activity level using KOOS, Tegner Activity Scale, Lysholm Score and ACL-RSI.<br>- Recording of the re-injury rate<br>- Assessment of health-related quality of life using SF 12