Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
NYU Langone Health
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients at Risk:
Diagnosed of primary symptomatic cervical degenerative disc disease confirmed with appropriate imaging studies.
Etiologies will be limited to cervical disc herniation, spinal stenosis, low-grade (I and II) spondylolisthesis, spondylosis and degenerative disc disease.
Will be undergoing elective cervical spine surgery, not to exceed 5 levels.
Presence of both axial (neck pain) and appendicular (arm pain/dysesthesia/weakness) symptoms, regardless of proportion
Subject must be able to be contacted by telephone during study participation
NDI \> 20%
Read and comprehend English
Diagnosed of primary symptomatic cervical degenerative disc disease confirmed with appropriate imaging studies.
Etiologies will be limited to cervical disc herniation, spinal stenosis, low-grade (I and II) spondylolisthesis, spondylosis and degenerative disc disease.
Will be undergoing elective cervical spine surgery, not to exceed 5 levels.
Presence of both axial (neck pain) and appendicular (arm pain/dysesthesia/weakness) symptoms, regardless of proportion
Subject must be able to be contacted by telephone during study participation
NDI \> 20%
Read and comprehend English
You may not be if
Contraindicated to surgical treatment of the cervical spine.
Prior cervical fusion
Evidence of severe cervical spinal deformity based on Ames classification: C2-C7 SVA \> 8cm, Horizontal Gaze \< -10 or \> 25, T1S-CL \> 20, myelopathy (JOA score \<10) or severe adult spinal deformity based on SRS-Schwab classification (PI-LL \> 20, PT \>30, SVA \> 90 mm)
Undergoing simultaneous treatment for thoracolumbar spine related diagnoses at the time of enrollment History of any spinal surgery within the last 6 months
Patients with neck pain attributable to trauma, idiopathic deformity, neoplasm, osteoporosis, or other medical condition.
Unlikely to comply with the follow-up evaluation schedule
Subject has recent history of chemical substance dependency that may impact the outcome or study participation
Contraindicated to surgical treatment of the cervical spine.
Prior cervical fusion
Evidence of severe cervical spinal deformity based on Ames classification: C2-C7 SVA \> 8cm, Horizontal Gaze \< -10 or \> 25, T1S-CL \> 20, myelopathy (JOA score \<10) or severe adult spinal deformity based on SRS-Schwab classification (PI-LL \> 20, PT \>30, SVA \> 90 mm)
Undergoing simultaneous treatment for thoracolumbar spine related diagnoses at the time of enrollment History of any spinal surgery within the last 6 months
Patients with neck pain attributable to trauma, idiopathic deformity, neoplasm, osteoporosis, or other medical condition.
Unlikely to comply with the follow-up evaluation schedule
Subject has recent history of chemical substance dependency that may impact the outcome or study participation
Subject has a significant psychosocial disturbance or psychiatric history that may impact the outcome or study participation including a DRAM score over 33
Active infection
Systemic infection (AIDS, HIV, or active hepatitis)
