Ignite Creation Date:
2024-05-06 @ 2:48 AM
Last Modification Date:
2024-10-26 @ 11:24 AM
Study NCT ID:
NCT02139527
Status:
TERMINATED
Last Update Posted:
2014-05-15
First Post:
2014-02-11
Brief Title:
CARES Lumbar Artificial Disc Registry
Sponsor:
DePuy Spine
Organization:
DePuy Spine
Study Overview
Official Title:
The Centers for Arthroplasty Research and Education in Spine CARES Lumbar Artificial Disc Registry Protocol
Status:
TERMINATED
Status Verified Date:
2014-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Low enrollment and follow-up data on enrolled patients
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None