Trials / Terminated
TerminatedNCT02139527
CARES Lumbar Artificial Disc Registry
The Centers for Arthroplasty Research and Education in Spine (CARES) Lumbar Artificial Disc Registry Protocol
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 120 (actual)
- Sponsor
- DePuy Spine · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of the registry is to assess outcomes following treatment with lumbar total disc replacement (TDR) in patients outside the clinical trial setting.
Detailed description
The purpose of this study is to capture outcomes associated with use of total disc replacement (TDR) in patients treated with either the CHARITE™ Artificial Disc or the PRODISC®-L Total Disc Replacement may be included in the registry.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Total Disc Replacement |
Timeline
- Start date
- 2007-05-01
- Primary completion
- 2009-08-01
- Completion
- 2009-08-01
- First posted
- 2014-05-15
- Last updated
- 2014-05-15
Source: ClinicalTrials.gov record NCT02139527. Inclusion in this directory is not an endorsement.