Trials / Recruiting
RecruitingNCT05653102
A Post-Market Domestic (US) and International Data Collection to Assess the Truliant Knee System
CR17-003 Truliant Knee PMCF: A Post-Market Domestic (US) and International Data Collection to Assess the Truliant Knee System
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 1,000 (estimated)
- Sponsor
- Exactech · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A Post-Market Domestic (US) and International Data Collection to Assess the Truliant® Knee System
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).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Truliant Total Knee System | Total Knee Arthroplasty using Exactech's Truliant® branded components are compatible with Optetrak branded components. |
Timeline
- Start date
- 2019-01-23
- Primary completion
- 2035-01-31
- Completion
- 2035-07-31
- First posted
- 2022-12-16
- Last updated
- 2024-06-18
Locations
5 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05653102. Inclusion in this directory is not an endorsement.