clinical trial · NCT05653102
A Post-Market Domestic (US) and International Data Collection to Assess the Truliant Knee System
Exactech·—·recruiting·n = 1,000
Knee Arthroplasty, TotalTruliant Total Knee System
brief summary
A Post-Market Domestic (US) and International Data Collection to Assess the Truliant® Knee System
started
Jan 23, 2019
primary completion
Jan 31, 2035
completion
Jul 31, 2035
last updated
Jun 18, 2024
detailed 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).
official title
CR17-003 Truliant Knee PMCF: A Post-Market Domestic (US) and International Data Collection to Assess the Truliant Knee System
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol