Trials / Completed
CompletedNCT00487565
Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System
LCS® PS: A Prospective, Multi-center Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 210 (actual)
- Sponsor
- DePuy Orthopaedics · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Prospective, multi-center clinical study to evaluate the clinical outcomes of the posterior stabilized design of the LCS® Complete Mobile-bearing Total Knee System
Detailed description
Prospective, multi-center study to evaluate the clinical outcome of posterior stabilized design of LCS® Complete Mobile-Bearing Total Knee System. No comparison group. 12 month enrollment, 12 month post-operative evaluation. Follow-up intervals: Pre-op, 3 month, 6 month, and 12 month.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Total knee arthroplasty | Total knee arthroplasty using a posterior stabilized implant |
Timeline
- Start date
- 2006-09-01
- Primary completion
- 2011-02-01
- Completion
- 2011-02-01
- First posted
- 2007-06-18
- Last updated
- 2013-08-14
- Results posted
- 2012-03-23
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00487565. Inclusion in this directory is not an endorsement.