Optetrak Knee System Post Market Clinical Follow-Up

Running, not enrolling

Conditions studied: Knee Arthroplasty, Total

In brief

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

Key facts

Study ID

NCT05788757

Run by

Exactech

People needed

4588

Starts

2011-06-01

Expected to finish

2034-06-01

Last updated by the study team

2024-06-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient is indicated for knee replacement, or has already undergone knee replacement, with a device manufactured or distributed by Exactech
• Patient is skeletally mature
• Patient meets the indications detailed in the applicable product package insert Patient is willing and able to review and sign an informed consent form, if necessary

You may not qualify if…

• Patient has a local or systemic infection
• Patient has a known sensitivity to one or more of the materials in the knee replacement system to be used
• Patient is pregnant
• Patient has a mental or physical condition that may invalidate evaluation of the data - ---
• Patient is a prisoner
• Surgery is contraindicated according to the applicable product package insert

Where it is running

• Fallon Clinic — Worcester, Massachusetts, United States
• Nevada Orthopaedic and Spine Center — Las Vegas, Nevada, United States
• Medical University South Carolina — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.