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Interference Screw Mectascrew-B Postmarket Study

NCT06166784 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 27

Last updated 2023-12-12

No results posted yet for this study

Summary

An observational prospective study with the aim to assess the clinical outcomes at 1year after surgery for a specific composite IS (Medacta Mectascrew B) in the reconstructive treatment of ruptured ACL or PCL by means of an autograft or allograft.

Conditions

  • Anterior Cruciate Ligament Injuries Posterior Cruciate Ligament Tear

Interventions

DEVICE

Mectascrew B

reconstruction of ACL or PCL rupture

Sponsors & Collaborators

  • Medacta International SA

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-19
Primary Completion
2025-11-30
Completion
2026-01-31
FDA Device
Yes

Countries

  • Germany

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06166784 on ClinicalTrials.gov