Ignite Creation Date:
2024-05-06 @ 8:06 AM
Last Modification Date:
2024-10-26 @ 11:56 AM
Study NCT ID:
NCT02667067
Status:
COMPLETED
Last Update Posted:
2022-06-30
First Post:
2015-10-08
Brief Title:
Investigation of the Simplify Cervical Artificial Disc
Sponsor:
NuVasive
Organization:
NuVasive
Study Overview
Official Title:
Clinical Study Protocol for the Investigation Of The Simplify Cervical Artificial Disc
Status:
COMPLETED
Status Verified Date:
2022-06
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:
This study is intended to demonstrate that the Simplify Disc is at least as safe and effective as conventional anterior cervical discectomy and fusion ACDF when used to treat one level between C3 to C7 for cervical degenerative disc disease DDD defined as intractable radiculopathy arm pain andor a neurological deficit with or without neck pain or myelopathy due to a single-level abnormality localized to the level of the disc space in subjects who are unresponsive to conservative management
Detailed Description:
The objective of this clinical study is to evaluate the safety and effectiveness of the Simplify Disc for treatment of DDD compared to conventional ACDF for reconstruction of the disc space at one level between C3 to C7 for DDD defined as intractable radiculopathy arm pain andor a neurological deficit with or without neck pain or myelopathy due to a single-level abnormality localized to the level of the disc space that is unresponsive to conservative management
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