Trials / Completed
CompletedNCT00726128
Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
A Multi-Center Prospective Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 371 (actual)
- Sponsor
- Zimmer Biomet · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
To prospectively collect radiographic and outcome data on patients who are having cervical spine fusion surgery with the VueLock™ Anterior Cervical Plate System
Detailed description
The purpose is to prospectively collect radiographic and outcome data on patients who are having cervical spine fusion surgery with the VueLock™ Anterior Cervical Plate System.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | VueLock™ Anterior Cervical Plate | Implanted in subjects having an ACDF (Anterior cervical discectomy and fusion) |
Timeline
- Start date
- 1998-08-01
- Primary completion
- 2009-09-01
- Completion
- 2009-09-01
- First posted
- 2008-07-31
- Last updated
- 2020-02-24
Locations
4 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00726128. Inclusion in this directory is not an endorsement.