Cervical Interbody Implant Study for Degenerative Disc Disease and Cervical Spinal Instability
This study is looking at the safety and performance of cervical spine surgery using specific interbody implants (Cohere Cervical or Modulus Cervical) in people with degenerative disc disease or cervical spinal instability. You could join if you are at least 18 years old and are planning to have cervical spine surgery using one of these implants. The study will look at how many complications happen and how well the bones fuse together after surgery, over 24 months. The study is currently unclear on its recruitment status and plans to enroll at least 150 participants.
- Study design
- This is an observational study that will follow at least 150 participants, with 75 in each implant group, for 24 months.
- What's involved
- You would undergo interbody fusion surgery using one of the specified implants as part of your surgeon's standard care.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for 24 months after surgery to check for complications and fusion success.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Cervical Interbody Implant Study
At a glance
Conditions
NCT04689854
Where you'd take part
This study runs at 7 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Columbia Orthopedic Group Research
Columbia, Missourino site contact published
Duke University
Durham, North Carolinano site contact published
Hartford Healthcare Bone and Joint Institute
Hartford, Connecticutno site contact published
Mass General Brigham
Somerville, Massachusettsno site contact published
Orthopedic Specialty Institute
Orange, Californiano site contact published
Summa Health
Akron, Ohiono site contact published
University of Virginia
Charlottesville, Virginiano site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Kyle Malone, MS · STUDY_DIRECTOR · Globus Medical
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Complications of Interbody Implants24 months
Rate of complications (i.e., safety) attributable to the use of the interbody implants to be studied.
- Radiographic Fusion Success24 months
The proportion of subjects with apparent radiographic fusion (i.e., performance) of the index surgical level(s) at 24 months postoperative.