Trials / Completed
CompletedNCT01301950
Comparison of Surgical Time and Efficiency of Total Knee Arthroplasty
Comparison of Surgical Time and Efficiency of Total Knee Arthroplasty Using TruMatch® Personalized Solutions Compared to Conventional Total Knee Arthroplasty
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- DePuy Orthopaedics · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This study is designed to compare the surgical efficiency of TruMatch® Personalized Solutions surgical technique compared to conventional surgical technique. Specifically, the purpose of this study is to collect time data to enhance the existing economic model.
Detailed description
The study is designed as a prospective, multi-center, controlled, non-randomized, clinical investigation to compare the efficiency of TruMatch® Personalized Solutions surgical technique compared to conventional surgical technique.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Custom Patient Instrumentation | TruMatch® Personalized Solutions is the brand name of DePuy Orthopaedics, Inc. custom patient instrumentation (CPI). TruMatch™ is a pair of custom-made cutting blocks that allow distal femoral and proximal tibial cuts to be made according to a predefined surgical plan. The inner surface of the femoral block is manufactured to match the geometry of the patient's distal femur. The inner surface of the tibial block is manufactured to match the patient's proximal tibia. The geometric data is obtained from a CT scan and a preoperative plan approved by the surgeon |
| OTHER | Conventional Instruments | Total Knee Arthroplasty implanted using conventional instruments (non-CPI) and surgical technique. |
Timeline
- Start date
- 2010-05-01
- Primary completion
- 2013-08-01
- Completion
- 2013-08-01
- First posted
- 2011-02-23
- Last updated
- 2019-04-10
- Results posted
- 2014-09-05
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01301950. Inclusion in this directory is not an endorsement.