Ignite Creation Date:
2024-05-05 @ 5:24 PM
Last Modification Date:
2024-10-26 @ 9:31 AM
Study NCT ID:
NCT00443547
Status:
COMPLETED
Last Update Posted:
2019-07-29
First Post:
2007-03-02
Brief Title:
Outcome Study of Patients Treated With Translational Cervical Plate Used to Treat Degenerative Disc Disease
Sponsor:
Synthes USA HQ Inc
Organization:
Synthes USA HQ Inc
Study Overview
Official Title:
Prospective Multi-Center Clinical Study of Patients With Degenerative Disc Disease Treated With Anterior Cervical Decompression and Fusion Using the Vectra-T Translational Cervical Plate
Status:
COMPLETED
Status Verified Date:
2019-06
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 purpose of this study is to measure the benefits of anterior from the front cervical neck surgery for degenerative disc disease The research part of this study is the answering of questionnaires by the patient concerning their quality of life prior to and after surgery
Detailed Description:
This is a prospective multi-center four-arm study designed to evaluate the clinical and radiographic outcomes in patients diagnosed with cervical degenerative disc disease DDD and treated using the Vectra-T Cervical Plate and the Advanced ACF or CorticoCancellous Allograft Spacer made by Synthes Spine Company Paoli PA This is not an investigational study IDE and no investigational or experimental devices or procedures are included in this study
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