Trials / Terminated
TerminatedNCT01092312
Signature Personalised Patient Care System With the Vanguard Knee System Study
Study on the Signature Personalised Patient Care System With the Vanguard Knee System
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 325 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine whether the percentage cases which have ideal mechanical axial alignment using the Vanguard total Knee implant with the Signature cutting blocks is higher than those without the use of Signature when measured immediately post-operatively.
Detailed description
The purpose of this study is to determine whether the percentage cases which have ideal mechanical axial alignment using the Vanguard total Knee implant with the Signature cutting blocks is higher than those without the use of Signature when measured immediately post-operatively. Other outcomes will include knee assessments and patient questionnaires.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Vanguard Knee System with Signature Knee Guide | Use of Signature Knee Guide |
| PROCEDURE | Vanguard Knee System with conventional Instruments | Vanguard Knee System with conventional Instruments |
Timeline
- Start date
- 2010-03-01
- Primary completion
- 2016-09-01
- Completion
- 2016-09-01
- First posted
- 2010-03-24
- Last updated
- 2017-09-05
Locations
12 sites across 10 countries: United States, Australia, Austria, Belgium, Denmark, France, Netherlands, Portugal, Sweden, United Kingdom
Source: ClinicalTrials.gov record NCT01092312. Inclusion in this directory is not an endorsement.