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

Biomatlante55 enrolled

Overview

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

Study Type

OBSERVATIONAL

Enrollment

Conditions

Knee Ligament Injury

Interventions

Anterior Cruciate Ligament ReconstructionDEVICE

Reconstruction of the Anterior Cruciate Ligament using an interference screw

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Acute or chronic ACL deficiency with complete or partial lesion of the anteromedial bundle requiring primary reconstruction of the Anterior Cruciate Ligament with hamstring tendons * Males or females aged froù 18 to 60 years * No history of surgery on the affected knee * Patients not under guardianship or judicial protection * Signature of non opposition form (consent of the patient Exclusion Criteria: * History of ligament, meniscal surgery or fracture of the affected knee * Pregnancy of breastfeeding women

Outcomes

Primary Outcomes

Change of the objective International Knee Documentation Committee score before and after surgery

Record of the objective International Knee Documentation Committee score (A = normal, B = almost normal, C = abnormal or D = very abnormal)

Time frame: 4 months before surgey / 7 months post-surgery

Change of the subjective International Knee Documentation Committee score before and after surgery

Record of the subjective International Knee Documentation Committee score (from 1 to 100 where 100 is the best result)

Time frame: 4 months before surgey / 7 months post-surgery

Secondary Outcomes

Number and precise description of any adverse event during the follow-up

Record and description of any adverse event during the follow-up that reflects the safety of the Composite Interference Screw

Time frame: Before surgery until 7 months post-surgery

Change in the patients recovery

Record of recovery informations

Time frame: 2 months post-surgery