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Knee Ligament Injury clinical trials

View clinical trials related to Knee Ligament Injury.

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NCT ID: NCT04122677 Recruiting - Clinical trials for Knee Ligament Injury

Performance and Safety of the Polylactic Interference Screw Used in Anterior Cruciate Ligament Reconstructions

Start date: November 14, 2019
Phase:
Study type: Observational

The evaluation of the clinical data has demonstrated the conformity of the Polylactic Interference Screw (PIS), with the relevant essential requirements for its use in orthopaedic applications. The Polylactic Interference Screws are intended for tibial and femoral ligament/graft fixation in the case or Anterior Cruciate Ligament (ACL) reconstructions. It has been concluded that the risks associated with the use of the device are acceptable when weighted against the benefits to the patients. In order to improve the clinical data on the PIS, the manufacturer, Biomatlante, decided to assess that the performance and safety of the device are maintained until the reaching of its intended use. In this objective, the goal of this study will be to observe the following parameters: Objective IKDC score (clinical evaluation) Subjective IKDS score (functional evaluation) Safety (report of any adverse event) Follow-up of the patient's recovery

NCT ID: NCT04076956 Recruiting - Clinical trials for Knee Ligament Injury

Performance and Safety of the Composite Interference Screw Used in Anterior Cruciate Ligament Reconstructions

Start date: August 23, 2019
Phase:
Study type: Observational

The evaluation of the clinical data has demonstrated the conformity of the Composite Interference Screw (CIS), with the relevant essential requirements for its use in orthopaedic applications. The Composite Interference Scres are intended for tibial and femoral ligament/graft fixation in the case or Anterior Cruciate Ligament (ACL) reconstructions. It has been concluded that the risks associated with the use of the device are acceptable when weighted against the benefits to the patients. In order to improve the clinical data on the CIS, the manufacturer, Biomatlante, decided to assess that the performance and safety of the device are maintained until the reaching of its intended use. In this objective, the goal of this study will be to observe the following parameters: 1. Objective IKDC score (clinical evaluation) 2. Subjective IKDS score (functional evaluation) 3. Safety (report of any adverse event) 4. Follow-up of the patient's recovery