Ignite Creation Date:
2024-05-06 @ 2:58 PM
Last Modification Date:
2024-10-26 @ 1:41 PM
Study NCT ID:
NCT04489394
Status:
COMPLETED
Last Update Posted:
2024-04-09
First Post:
2020-07-24
Brief Title:
Quintex Follow-up After One Year Minimum
Sponsor:
Aesculap AG
Organization:
Aesculap AG
Study Overview
Official Title:
Prospective Follow-up Study of the Aesculap Quintex Anterior Cervical Plating System After a Minimum of One Year
Status:
COMPLETED
Status Verified Date:
2024-04
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:
Quintex
Brief Summary:
Prospective study not randomised non-interventional monocentric investigating an intended patient cohort of 60 patients already operated on the cervical spine due to degenerative disc disease of the cervical spine down to the first thoracolumbar VBR C2-T1 who received a Quintex plate for stabilisation
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None