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

Knee Arthroplasty, Total Clinical Trial

Official title:
CR17-003 Truliant Knee PMCF: A Post-Market Domestic (US) and International Data Collection to Assess the Truliant Knee System

Clinical Trial Summary

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

Clinical Trial Description

Patient outcomes data is important for assessing the post-market safety and effectiveness of orthopedic medical devices. The purpose of this study is to collect clinical and patient outcomes and survivorship data for patients who have received or will receive a Truliant® knee prosthesis manufactured or distributed by Exactech Inc (Gainesville, Florida, USA). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05653102
Study type Observational
Source Exactech
Contact Pearl Harris
Phone 352-327-4846
Email pearl.harris@exac.com
Status Recruiting
Phase
Start date January 23, 2019
Completion date July 31, 2035
View Details
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