Trials / Completed
CompletedNCT01338493
Maverick Total Disc Replacement in a 'Real World' Patient Population
Maverick Total Disc Replacement in a 'Real World' Patient Population - A Prospective, Multicenter, Observational Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 139 (actual)
- Sponsor
- Medtronic Spinal and Biologics · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The primary purpose of the study is to document the reduction of disability after Maverick total disc replacement surgery in a 'real-world' patient population requiring disc replacement.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | lumbar spinal arthroplasty + Maverick™ | All patients will be subjected to a lumbar spinal arthroplasty. The anterior lumbar spine is approached through either a transperitoneal or retroperitoneal exposure. A complete anterior discectomy is performed and the Maverick™ Artificial Disc System is inserted to replace the damaged lumbar intervertebral disc. |
Timeline
- Start date
- 2009-02-01
- Primary completion
- 2013-07-01
- Completion
- 2013-07-01
- First posted
- 2011-04-19
- Last updated
- 2016-01-28
- Results posted
- 2014-11-18
Locations
13 sites across 3 countries: Canada, France, Germany
Source: ClinicalTrials.gov record NCT01338493. Inclusion in this directory is not an endorsement.