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MOTO Post-marketing Surveillance Study

NCT04072055 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2023-03-20

No results posted yet for this study

Summary

The prospective, multicentric, observational study has the aims to monitor the performance of the MOTO medial unicompartmental knee system in the treatment of patients with knee disease requiring a UKA. 150 patients will be recruited in 18 months and will be reviewed until 5 years follow-up visit after surgery. The primary objective of the study is to evaluate the prosthesis survival at 5 years.

Conditions

  • Osteonecrosis
  • Osteo Arthritis Knee

Interventions

DEVICE

MOTO Medial

MOTO medial unicompartmental knee system

Sponsors & Collaborators

  • Medacta International SA

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-25
Primary Completion
2023-03-16
Completion
2023-03-16
FDA Device
Yes

Countries

  • Belgium

Study Locations

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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 NCT04072055 on ClinicalTrials.gov