Trials / Withdrawn
WithdrawnNCT01308515
Vanguard Knee Anterior Stabilized Versus Posterior Stabilized Bearing Study
A Comparative Clinical Evaluation of the Vanguard Knee System's Anterior Stabilized & Posterior Stabilized Tibial Bearings
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the performance of two FDA-cleared tibial bearings (replacement for cartilage in the knee) by collecting data on patients through 3 years of follow-up.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Vanguard Knee System with AS Bearing | FDA cleared Tibial bearing that stabilizes the knee with an anterior lip, and is used with FDA cleared Vanguard CR (Cruciate Retaining) Femoral Component. |
| DEVICE | Vanguard Knee System with PS Bearing | FDA cleared Tibial bearing that stabilizes the knee with a post that articulates with the FDA cleared Vanguard PS(Posterior Stabilizing) Femoral Component. |
Timeline
- Start date
- 2010-09-01
- Primary completion
- 2010-09-01
- Completion
- 2010-09-01
- First posted
- 2011-03-04
- Last updated
- 2017-06-21
Source: ClinicalTrials.gov record NCT01308515. Inclusion in this directory is not an endorsement.