This trial is active, not recruiting.

Condition degenerative disc disease (ddd)
Treatments fld, control
Sponsor AxioMed Spine Corporation
Start date September 2008
End date August 2016
Trial size 300 participants
Trial identifier NCT00775801, PR-125


This study will look at the result of using the FLD device as an artificial lumbar disc. The study will compare the safety and effectiveness of the FLD artificial lumbar disc to an already approved artificial lumbar disc.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Artificial lumbar disc
(Active Comparator)
Artificial lumbar disc

Primary Outcomes

Overall success will be determined by a composite of measures regarding subject self-assessment of function (disability), low back pain, neurological function and device implantation status.
time frame: 24 Months

Secondary Outcomes

The improvement of subject self-assessment of function (disability), low back pain, patient satisfaction, neurological function and device implantation status at the 24 month follow-up compared to baseline.
time frame: 24 Months

Eligibility Criteria

Male or female participants from 21 years up to 65 years old.

Inclusion Criteria: - Single level, degenerative disc disease at L3 to S1, inclusive. - Minimum of 6 months of unsuccessful conservative treatment. - Subject is a surgical candidate for an anterior approach to the lumbar spine (<3 abdominal surgeries). - Back pain at the operative level only (by discogram, if necessary). - Leg pain and/or back pain due to disc space settling, with or without radicular symptoms related to foraminal narrowing. - Subject must understand and sign the written Informed Consent. Exclusion Criteria: - Prior fusion at any lumbar level. - Clinical evidence of adjacent lumbar segment disease. - Previous trauma to the L3, L4, L5, or S1 levels (in compression or burst). - Non-contained or extruded herniated nucleus pulposus. - Congenital stenosis or central/lateral stenosis (mid-sagittal stenosis of <8mm by CT or MR) secondary to acquired degenerative disease requiring treatment that destabilizes the spine (requiring fusion), or for subjects in whom increased motion may increase symptoms. - Retro- or spondylolisthesis of ≥ 2.5 mm which is either fixed or present on flexion/extension films, and slippage of vertebral body where the listhesis is due to disc space settling in the absence of degenerative facets or a pars interarticularis defect. - Significant kyphosis (>11ْ sagittal plane deformity). - History of any invasive malignancy (except non-melanoma skin cancer) unless treated with curative intent and there have been no clinical signs or symptoms of malignancy for at least 5 years (in particular, spinal tumors). - Acute or chronic infection (local or systemic). - Instability or facet joint arthrosis, clinically significant. - Arachnoiditis. - Known or suspected allergy to titanium, polyurethane, cobalt, chromium, molybdenum or silicone. - Radiographic findings of a fused or total collapsed disc. - Subject using medications or drugs known to potentially interfere with bone or soft tissue healing (high-dose of steroids, osteoclast inhibitors, etc.). - Systemic disease affecting the spine, including rheumatoid arthritis, autoimmune disease, AIDS, HIV, or hepatitis. - Paget's disease, osteomalacia or any other metabolic bone disease (excluding osteoporosis which is addressed separately). - Psychosocial disorders (e.g. evidence or drug or alcohol abuse). - Morbid (extreme) obesity (BMI ≥ 40 kg/m2). - Bone growth stimulator use in spine. - Investigational drug or device use within 30 days. - Osteoporosis or osteopenia or metabolic bone disease as confirmed by DEXA scan if poor bone quality is suspected (T-score < -1.0). - If female of childbearing potential, pregnant or interested in becoming pregnant in the next three years. - Type 1 diabetes, and uncontrolled (or poorly controlled) Type 2 diabetes. - Subjects with a history of implant rejection. - Provocative discography with non-concordant pain at the operative level. - Incarcerated subjects. - Myelopathy. - Significant leg pain of a radicular or neurogenic claudication nature. - Involved vertebral endplates dimensionally smaller then 39 mm in the mediallateral and/or 32 mm in the anterior-posterior directions. - Subjects not able to meet follow-up requirements. - Lumbar scoliosis > 11 degrees. - Any previous or current litigation related to the spine.

Additional Information

Official title An IDE Study of the Freedom Lumbar Disc in the Treatment of Lumbar Degenerative Disc Disease
Description The Freedom Lumbar Disc is indicated for spinal arthroplasty in skeletally mature patients with single level, symptomatic degenerative disc disease (DDD) from L3-S1. This is a prospective, multi-center, randomized, controlled trial. Subjects with DDD will be randomized to disc arthroplasty with the FLD device or a control device. The overall purpose (objective) of this trial is to collect clinical data to demonstrate the safety and effectiveness of FLD used for the treatment of symptomatic lumbar degenerative disc disease compared to the control device.
Trial information was received from ClinicalTrials.gov and was last updated in July 2016.
Information provided to ClinicalTrials.gov by AxioMed Spine Corporation.