Ignite Creation Date:
2024-05-05 @ 4:43 PM
Last Modification Date:
2024-10-26 @ 9:23 AM
Study NCT ID:
NCT00291018
Status:
COMPLETED
Last Update Posted:
2017-11-20
First Post:
2006-02-10
Brief Title:
Safety and Efficacy Study Comparing ProDisc-C to ACDF Surgery to Treat SCDD
Sponsor:
Synthes USA HQ Inc
Organization:
Synthes USA HQ Inc
Study Overview
Official Title:
A Multi-Center Prospective Randomized Controlled Clinical Trial Comparing the Safety and Effectiveness of ProDisc-C to Anterior Cervical Discectomy and Fusion ACDF Surgery in the Treatment of Symptomatic Cervical Disc Disease SCDD
Status:
COMPLETED
Status Verified Date:
2017-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The objective of this clinical investigation is to compare the safety and effectiveness of ProDisc-C to anterior cervical discectomy and fusion ACDF surgery in the treatment of symptomatic cervical disc disease SCDD
Detailed Description:
None
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