Clinical Trials Directory

Trials / Completed

CompletedNCT04122677

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

Status
Completed
Phase
Study type
Observational
Enrollment
55 (actual)
Sponsor
Biomatlante · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DEVICEAnterior Cruciate Ligament ReconstructionReconstruction of the Anterior Cruciate Ligament using an interference screw.

Timeline

Start date
2019-11-14
Primary completion
2022-12-21
Completion
2022-12-21
First posted
2019-10-10
Last updated
2025-02-04

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04122677. Inclusion in this directory is not an endorsement.