U.S., April 30 -- ClinicalTrials.gov registry received information related to the study (NCT07556978) titled 'Post-market Observational Clinical Study With the CE-marked Implantable Class IIb Medical Device "ITC CERVICAL"' on April 22.

Brief Summary: The goal of this observational post-market study is to evaluate the clinical performance and safety of the ITC CERVICAL device, a CE-marked implantable cervical interbody fusion cage, in adult patients undergoing anterior cervical discectomy and fusion (ACDF) for symptomatic cervical degenerative disc disease.

The main questions it aims to answer are:

1. Does the ITC CERVICAL device improve neck disability and pain after surgery?

2. Does the device demonstrate adequate radiological performa...