LDR Spine USA Mobi-C(R) Cervical Disc Prosthesis IDE
Degenerative Disc Disease
About this trial
This is an interventional treatment trial for Degenerative Disc Disease focused on measuring degenerative disc disease, cervical arthroplasty, Mobi C, multilevel, anterior cervical discectomy and fusion
Eligibility Criteria
Inclusion Criteria:
- Age 18-69 years.
Diagnosis of radiculopathy or myeloradiculopathy of the cervical spine, with pain, paresthesias or paralysis in a specific nerve root distribution C3 through C7, including at least one of the following:
- Neck and/or arm pain (at least 30mm on the 100mm VAS scale).
- Decreased muscle strength of at least one level on the clinical evaluation 0 to 5 scale.
- Abnormal sensation including hyperesthesia or hypoesthesia; and/or
- Abnormal reflexes
- Symptomatic at one or two adjacent levels from C3 to C7;
Radiographically determined pathology at one or two adjacent level(s) to be treated correlating to primary symptoms including at least one of the following:
- Decreased disc height on radiography, CT, or MRI in comparison to a normal adjacent disc.
- Degenerative spondylosis on CT or MRI.
- Disc herniation on CT or MRI;
- Neck Disability Index Score of ≥15/50 or ≥30%;
Unresponsive to non-operative, conservative treatment (rest, heat, electrotherapy, physical therapy, chiropractic care and/or analgesics) for:
- Approximately six weeks from radiculopathy or myeloradiculopathy symptom onset; or
- Have the presence of progressive symptoms or signs of nerve root/spinal cord compression despite continued non-operative conservative treatment.
Note: Not a complete listing
Exclusion Criteria:
- Reported to have an active systemic infection or infection at the operative site;
- Reported to have a history of or anticipated treatment for active systemic infection, including HIV or Hepatitis C;
- More than one immobile vertebral level between C1 to C7 from any cause including but not limited to congenital abnormalities and osteoarthritic "spontaneous" fusions;
- Previous trauma to the C3 to C7 levels resulting in significant bony or disco-ligamentous cervical spine injury;
- Reported to have had any prior spine surgery at the operative level;
- Reported to have had prior cervical fusion procedure at any level;
- Axial neck pain in the absence of other symptoms of radiculopathy or myeloradiculopathy justifying the need for surgical intervention;
- Disc height less than 3mm as measured from the center of the disc in a neutral position and disc height less than 20% of the anterior-posterior width of the inferior vertebral body;
- Radiographic confirmation of severe facet joint disease or degeneration;
Note: Not a complete listing
Sites / Locations
- Texas Back Institute-West
- Southern California Institute of Neurological Surgery
- Massoudi & Jackson Neurosurgical Association
- Memorial Orthopaedic Surgical Group
- Eisenhower Medical Center
- University of California- Davis Medical Center
- Spine Institute at St. John's Health Center
- Stanford University
- Panorama Orthopedics and Spine Care
- Southeastern Clinical Research
- Orthopaedics North East
- Spine Institute of Louisiana
- GBMC Healthcare
- University Neurologic Systems
- St. Mary's of Saginaw Field Neurosciences Institute
- Simmons Orthopaedics and Spine Associates
- Orthopedic Spine Care of Long Island
- The Cleveland Clinic
- Oklahoma Spine & Brain Institute
- Austin Brain and Spine
- Foundation Surgical Hospital
- West Texas Spine
- Texas Back Institute
- Texas Spine and Joint Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
1 Level
2 Level
Cervical artificial disc (investigational device) at 1 level compared with control procedure (ACDF) at one level
Cervical artificial disc (investigational device) at 2 levels compared with control procedure (ACDF) at two levels