Trials / Completed
CompletedNCT04321356
Analysis of Competitive Posterior Cruciate Retaining (PCR) and Posterior Stabilized (PS) Total Knee Arthroplasty (TKA)
Analysis of Competitive PCR and PS Total Knee Arthroplasty
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- The University of Tennessee, Knoxville · Academic / Other
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the study is to acquire kinematic in vivo fluoroscopy data from subjects who were implanted with Stryker Posterior Cruciate Retaining (PCR) , Stryker Posterior Stabilized (PS), Zimmer PCR, and Zimmer PS Total Knee Arthroplasty (TKAs). Our lab has previously collected data for the Smith \& Nephew PCR, bi-cruciate retaining (BCR), and bi-cruciate stabilized (BCS) TKA.
Detailed description
The objective for this study is to analyze the in vivo kinematics for subjects implanted with either a Stryker PCR, Stryker PS, Zimmer PCR, and Zimmer PS TKA and to compare those patterns to subjects having a normal knee from our previous study and to those patterns from subjects having a Smith \& Nephew PCR, BCR, and BCS TKA.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Triathlon PCR TKA | Total Knee Arthroplasty System |
| DEVICE | Triathlon PS TKA | Total Knee Arthroplasty System |
| DEVICE | Persona PCR TKA | Total Knee Arthroplasty System |
| DEVICE | Persona PS TKA | Total Knee Arthroplasty System |
Timeline
- Start date
- 2020-02-24
- Primary completion
- 2022-05-16
- Completion
- 2022-05-16
- First posted
- 2020-03-25
- Last updated
- 2023-11-28
- Results posted
- 2023-11-28
Locations
2 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04321356. Inclusion in this directory is not an endorsement.