Trials / Terminated
TerminatedNCT00588887
Total Knee Replacement With Duracon® and Vanguard™ Prostheses
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 150 (actual)
- Sponsor
- Biomet Orthopedics, LLC · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare range of motion, Knee Society Scores, and duration of surgery for different total knee prostheses.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Duracon® | This group utilizes the Duracon® prostheses for total knee replacement. |
| DEVICE | Vanguard™ | This group will utilize the Vanguard™ prostheses for total knee replacement. |
Timeline
- Start date
- 2005-06-01
- Primary completion
- 2008-02-01
- Completion
- 2008-06-01
- First posted
- 2008-01-09
- Last updated
- 2017-06-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00588887. Inclusion in this directory is not an endorsement.