Anterior Cruciate Ligament Rupture Clinical Trial
Official title:
ACL Reconstruction With Human Allograft Cortical Bone Screw (Shark Screw®) or Biocomposite-interference Screws - a Prospective, Randomized, Controlled Trial.
The goal of this clinical trial is to compare the outcome of 2 different screws for Anterior cruciate ligament reconstruction. The main question is if the human allogeneic cortical bone screw reduces tunnel widening in comparison to conventional treatment with a biocomposite screw. Additional the re-rupture rate will be evaluated and knee scores will be recorded before surgery and after surgery. Participants will have MRI before and after surgery, 3, 6, 12, and 24 months after surgery and Computertomography after surgery, 3, 6 and 24 months after surgery. Questionnaires (Knee-scores) will be recorded before surgery, 6, 12, 24 months after surgery. the investigators hope that with the human cortical bone screw the tunnel widening is reduced and the re-rupture rate is low
Status | Not yet recruiting |
Enrollment | 80 |
Est. completion date | June 1, 2031 |
Est. primary completion date | June 1, 2031 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - MRI-verified rupture of the anterior cruciate ligament - Indication for replacement surgery - Surgery within 6 months of injury - Uninjured contralateral knee Exclusion Criteria: - Previous rupture of the anterior cruciate ligament on the side to be operated on (rerupture) - Primary bone disease - inflammatory disease - Unstable meniscus - complete rupture of a collateral ligament - early rerupture during the examination period (early rerupture) |
Country | Name | City | State |
---|---|---|---|
Austria | Bezirkskrankenhaus Schwaz Betriebsgesellschaft m.b.H | Schwaz | Tirol |
Austria | Bezirkskrankenhaus Schwaz Betriebsgesellschaft m.b.H. | Schwaz | Tirol |
Lead Sponsor | Collaborator |
---|---|
Bezirkskrankenhaus Schwaz |
Austria,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | bone tunnel widening will be measured by CT and/or MRI and measured in mm | bone tunnel widening will be evaluated and measured by CT and/or MRI and measured in mm | immadiately after surgery, 3, 6, 12 and 24 months after surgery. | |
Secondary | International Knee Documentation Committee (IKDC) Scores | IKDC will be evaluated by questionnaires, it can be between 0 and 100 the higher the better is the outcome | before surgery and 6, 12 and 24 months after surgery | |
Secondary | Knee Injury and Osteoarthritis Outcome Score (KOOS) Scores | KOOS Score will be evaluated by questionnaires, it can be between 0 and 100 the higher the better is the outcome | before surgery and 6, 12 and 24 months after surgery | |
Secondary | Lysholm Knee Score | Lysholm Knee Score will be evaluated by questionnaires, one of the most frequently used assessment tools for the results of Anterior cruciate ligament reconstruction even though it only measures activities of daily living, it can be between 0 and 100 the higher the better is the outcome. | before surgery and 6, 12 and 24 months after surgery | |
Secondary | Tegner Activity Score | Tegner Activity Score will be evaluated by questionnaires | before surgery and 6, 12 and 24 months after surgery |
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