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RecruitingNCT04462458

M-ARS ACL Post-marketing Surveillance Study

Clinical and Radiological Outcomes of M-ARS ACL

Status
Recruiting
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
Medacta International SA · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to evaluate the performance of Medacta Anatomic Ribbon Surgery (M-ARS) in patients requiring anterior cruciate ligament (ACL) reconstruction. The main goal is to evaluate the survival rate of M-ARS ACL at 6 months post-operatively. The secondary goals are to assess the survival rate, clinical and functional outcomes, the quality of life, and the rate of complications at 1 month, 1 year and 2 years post-operatively.

Detailed description

This s a prospective, multicenter, non-controlled, observational study to evaluate the outcomes of Medacta Anatomic Ribbon Surgery (M-ARS) in the reconstruction of the anterior cruciate ligament (ACL). Participants will be informed about the study, both orally and in writing, during a preoperative visit. The investigator will answer any questions that may arise and will collect the informed consent. During the study, enrolled participants will be able to withdraw at any time and for any reason. The study is conducted according to the following schedule: * V1 : Inclusion during a preoperative visit * V2: Surgery * V3: Follow-up visit at 1 month ± 15 days post-surgery * V4: Follow-up visit at 6 months ± 30 days post-surgery * V5: Follow-up visit at 12 months ± 60 days post-surgery * V6: Follow-up visit at 24 months ± 90 days post-surgery The following data will be collected: * Survival rate of implants evaluating the incidence of implants failure, where implant failure is defined as revision, loosening, or any definite change in the position of components (V3-V6). * Clinical and functional outcomes, measured with the International Knee Documentation Committee (IKDC) score (V1, V3-V6) * Quality of Life, measured with the EQ-5D score (V1, V3-V6) * Occurrence of intraoperative and postoperative complications (V2-V6) Depending on standard practice, imaging assessment of implants and bone tunnels may be performed. A web-based data collection tool will be used as Electronic Data Capture (EDC). All the information required by the protocol will be collected in electronic case report forms (eCRF). The statistical analysis will be performed according to a pre-established statistical analysis plan. Missing values will not be replaced by estimated values but will be considered as missing in the statistical analysis.

Conditions

Interventions

TypeNameDescription
DEVICEMedacta Anatomic Ribbon Surgery (M-ARS ACL)M-ARS ACL allows to reconstruct the anterior cruciate ligament using the Anatomic Ribbon Technique

Timeline

Start date
2022-07-01
Primary completion
2025-07-01
Completion
2027-01-01
First posted
2020-07-08
Last updated
2023-03-13

Locations

3 sites across 2 countries: Austria, Germany

Source: ClinicalTrials.gov record NCT04462458. Inclusion in this directory is not an endorsement.