BRYAN Clinical Trial
Title: Post Approval Study: BRYAN® Cervical Disc
Study Sponsor: Medtronic Sofamor Danek
Principal Investigator: Christopher Rumana, MD
Study Synopsis: The goal of this post-approval study is to assess longer-term performance of the BRYAN® Cervical Disc in the treatment of patients with cervical degenerative disc disease. The study will be comprised of the investigational and control patients from the original IDE clinical trial for the BRYAN® Cervical Disc device as well as patients who received this device as part of the continued access arm.
Study Status: For more information, contact by e-mail April Bell, MS, CCRC at abell
tnc-neuro
com (abell
tnc-neuro
com) , or contact her by phone at 850-558-1230.
