Degenerative Disc Disease, Spondylolisthesis, Stenosis
Conditions
Brief summary
The primary objective of this study is to evaluate the safety and performance of the Modulus ALIF System in patients undergoing anterior lumbar interbody fusion (ALIF) as measured by reported complications, radiographic outcomes, and patient-reported outcomes.
Detailed description
Patients considered for this study will have previously undergone surgery for their spinal condition according to the standard of care of the practitioner. All patients at a given site who meet eligibility requirements will be considered for participation in the study. Available progress notes, medical records, patient-reported outcomes, radiographs (plain film and CT scans, if available), and complications will be obtained from the medical records of all enrolled subjects. The complication profile and overall performance of the Modulus ALIF System will be assessed using the following: 1. Complications attributable to the use of the Modulus ALIF System as noted in surgical summaries, progress notes, and hospital records; and 2. Radiographic outcome (fusion) and description of device status from available plain film radiographs and CT scan(s); and 3. Neurologic status, symptoms, and/or subject self-reported clinical outcomes (e.g., pain and disability), as available
Interventions
DEVICEModulus ALIF System
The Modulus ALIF System is designed to address lumbar pathologies utilizing interbody placement through an anterior or anterolateral surgical approach. The Modulus ALIF System is an interfixated interbody system available in various shapes and sizes to suit the individual pathology and anatomical conditions of the patient.
Sponsors
NuVasive
Study design
Observational model
COHORT
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Inclusion criteria
1. Availability of progress notes and radiographic information preoperatively and a minimum of 6 months following surgery 2. Male or female patients who are ≥18 years of age at the time of surgery 3. Had undergone a regiment of at least six (6) months of nonoperative care treatment prior to being treated with the Modulus ALIF system, except in patients with progressive neurological deficits, neurogenic claudication causing significant disability, or developed cauda equine syndrome 4. Treated with ALIF procedure with the Modulus ALIF System at: * One or two adjacent lumbar and/or lumbosacral levels for degenerative disc disease (DDD), degenerative spondylolisthesis, or spinal stenosis, or * Any number of lumbar and/or lumbosacral levels for degenerative scoliosis (defined as \>10º coronal curve) or sagittal deformity 5. Supplemental fixation cleared by the applicable regulatory body for use in the thoracolumbar spine unless the procedure meets all of the following criteria: * 1-2 levels treated for DDD, and * 3 or 4 interfixated screws placed, and * Implant lordosis is ≤20°
Exclusion criteria
1. Patient was a prisoner at the time of Modulus ALIF treatment 2. Patient was participating in another clinical study during treatment that would confound study data
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rates of complications attributable to the use of the Modulus ALIF System | 12 months |
| Proportion of subjects with apparent radiographic fusion at 6 months or greater postoperative | 12 months |
Secondary
| Measure | Time frame |
|---|---|
| Change in neurologic status, symptoms, and/or subject self-reported clinical outcomes (e.g., pain and disability), as available | 12 months |
Countries
United States
Outcome results
None listed