Optetrak Knee System Post Market Clinical Follow-Up

NCT05788757 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 4588

Last updated 2024-06-18

No results posted yet for this study

Summary

A Post-Market Domestic (US) and International Data Collection to Assess the Optetrak Knee System

Conditions

  • Knee Arthroplasty, Total

Interventions

DEVICE

Optetrak Total Knee System

Total Knee Arthroplasty using Exactech's Optetrak branded components.

Sponsors & Collaborators

  • Exactech

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-01
Primary Completion
2033-12-31
Completion
2034-06-01
FDA Device
Yes

Countries

  • United States

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 NCT05788757 on ClinicalTrials.gov