The aim of this study is to assess the clinical, biomechanical and functional outcome 2 years after anterior cruciate ligament (ACL) repair and InternalBraceTM augmentation now in direct comparison to ACL reconstruction and to identify potential deficits compared to the contralateral healthy side as well as with a knee-healthy age-matched collective. In addition, socio-economic aspects such as return to work and sports and treatment cost will be compared between both techniques.
Age range
18 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Range of Motion (ROM) of the knee
Timeframe: at baseline (2 years after surgery)
Isokinetic muscle strength
Timeframe: approx. 30 minutes at baseline (2 years after surgery)
Proprioception (joint position sense)
Timeframe: approx. 30 minutes at baseline (2 years after surgery)
Gait analysis
Timeframe: approx. 60 minutes at baseline (2 years after surgery)
Postural stability
Timeframe: at baseline (2 years after surgery)
Functional activity score to determine the ability "return to activity"
Timeframe: at baseline (2 years after surgery)