Trials / Active Not Recruiting
Active Not RecruitingNCT05788757
Optetrak Knee System Post Market Clinical Follow-Up
A Post-Market Domestic (US) and International Data Collection to Assess the Optetrak Knee System
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 4,588 (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 Optetrak 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 Optetrak® knee prosthesis manufactured or distributed by Exactech Inc (Gainesville, Florida, USA).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Optetrak Total Knee System | Total Knee Arthroplasty using Exactech's Optetrak branded components. |
Timeline
- Start date
- 2011-06-01
- Primary completion
- 2033-12-31
- Completion
- 2034-06-01
- First posted
- 2023-03-29
- Last updated
- 2024-06-18
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05788757. Inclusion in this directory is not an endorsement.