Trials / Withdrawn
WithdrawnNCT00808613
Optetrak Posterior Stabilized Versus Optetrak Hi-Flex
Prospective, Single-center, Non-randomized, Consecutive Series Study Comparing Functional Differences Between a Standard Posterior Stabilized TKR and a High-flexion Posterior Stabilized TKR
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Exactech · Industry
- Sex
- All
- Age
- 50 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the differences in clinical outcomes between the Optetrak® Posterior Stabilized ("Optetrak® PS", Exactech, Gainesville, FL) and the Optetrak® Hi-Flex™ ("Optetrak® HF", Exactech, Gainesville, FL) knee designs.
Detailed description
The purpose of this study is to evaluate the differences in clinical outcomes between the Optetrak® Posterior Stabilized ("Optetrak® PS", Exactech, Gainesville, FL) and the Optetrak® Hi-Flex™ ("Optetrak® HF", Exactech, Gainesville, FL) knee designs. The null hypothesis is that there is no difference in postoperative knee flexion between the Optetrak® PS and Optetrak® HF groups.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Optetrak PS | Optetrak Posterior Stabilized total knee replacement |
| DEVICE | Optetrak Hi-Flex | Optetrak Hi-Flex total knee replacement |
Timeline
- Start date
- 2008-12-01
- Primary completion
- 2012-01-01
- Completion
- 2012-01-01
- First posted
- 2008-12-16
- Last updated
- 2022-09-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00808613. Inclusion in this directory is not an endorsement.