Pilot Study of ZetaFuse™ Bone Graft for the Treatment of Cervical Degenerative Disc Disease

Overview

The goal of this pilot clinical trial is to test the safety and preliminary performance of the ZetaFuse Bone Graft in patient requiring fusion of the C3-C7 vertebral bones due to pain or loss of neurological function. Participants will be treated with ZetaFuse during surgical intervention to reduce pain and the loss of neurological function.

Detailed description

The indication under investigation is for use in the skeletally mature patients for fusion of one or two contiguous vertebral bodies in the cervical spine from C3-C7 following discectomy for intractable radiculopathy with or without neck pain, or myelopathy due to abnormality localized to the disc space and manifested by at least one of the following conditions confirmed by radiographic imaging:herniated nucleus pulposus, spondylosis (defined by the presence of osteophytes), and/or visible loss of disc height as compared to adjacent levels.

Interventions

• Device Cervical Fusion (ZetaFuse™ Bone Graft)
  Fusion of the C3-C7 cervical vertebral bodies

Primary outcome measures

• Subjects with Radiologic Determination of Bone Fusion of the Treated Cervical Vertebral Bones [Time frame: 1 year post surgery]

Secondary outcome measures (1)

• Quality of Life via Short Form (SF12v2) Health Survey [Time frame: 1 year post surgery]

Eligibility criteria

Inclusion criteria

• Age 22 to 75 years (inclusive) at the time of enrollment.
• Diagnosis of radiculopathy and/or myelopathy 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 3 on the 0 - 10 numeric rating scale for pain.
• 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 contiguous levels from C3 to C7.
• Radiographically determined pathology at the level to be treated correlating to primary symptoms including at least one of the following:

• Decreased disc height on radiography, computed tomography (CT), or magnetic resonance imaging (MRI) in comparison to a normal adjacent disc.
• Degenerative spondylosis on CT or MRI.
• Disc herniation on CT or MRI.
• Neck Disability Index Score ≥ 30/100.
• Unresponsive to non-operative treatment (e.g., rest, heat, physical therapy, chiropractor, massage, pain medication) for approximately six weeks from the symptom onset; or has the presence of progressive symptoms or signs of nerve root/spinal cord compression in the face of continued non-operative management.
• No previous surgical intervention at the involved levels or any subsequent, planned/staged surgical procedure at the involved or adjacent levels.
• Appropriate for treatment using an anterior surgical approach.
• Skeletally mature at the time of the surgery.
• Medically cleared for surgery.
• If a female of child-bearing potential, subject is non-pregnant, nonnursing, and agrees not to become pregnant during the study period.
• Willing and able to comply with the study plan.
• Signed written Patient Informed Consent Form.
• Willing to discontinue use of non-steroidal anti-inflammatory drugs (NSAIDs) from one week before the surgery to 3 months after the surgery.

Exclusion criteria

• A cervical spinal condition other than symptomatic cervical degenerative disc disease requiring surgical treatment at the involved levels.
• Documented or diagnosed cervical instability relative to adjacent segments at either level, defined by dynamic (flexion/extension) radiographs showing sagittal plane translation >3.5 mm or sagittal plane angulation > 20°.
• More than two cervical levels requiring surgical treatment.
• An immobile or spontaneously fused level adjacent to the levels to be treated.
• Severe pathology of the facet joints of the involved vertebral bodies.
• Previous surgical intervention at either one or both of the involved levels or at adjacent levels.
• History of trauma to the C3 to C7 levels resulting in significant bony or disco-ligamentous cervical spine injury.
• Previously diagnosed with osteomalacia;
• Any of the following that may be associated with an increased risk osteoporosis (if "Yes" to any of the below risk factors, a DEXA Scan is required to determine eligibility). If the level of bone mineral density (BMD) on DEXA scan is a T score of -2.5 or worse (i.e., -2.6, - 2.7, etc.) the subject is ineligible for the study.

• Postmenopausal non-Black female over 60 years of age who weighs less than 140 pounds.
• Postmenopausal female who has sustained a non-traumatic hip, spine, or wrist fracture.
• Male over the age of 60 who has sustained a non-traumatic hip or spine fracture.
• Taking bisphosphonate medication for the treatment of osteoporosis.
• Chronic use of high dose steroids.
• Reported active malignancy that included a history of any invasive malignancy (except non-melanoma skin cancer) unless the subject had been treated with curative intent and there had been no clinical signs or symptoms of the malignancy for at least five years.
• Overt or active systemic infection, or infection at the operative site.
• Insulin dependent diabetes.
• A tobacco user who does not agree to suspend smoking prior to surgery.
• Chronic or acute renal failure or prior history of renal disease.
• Mentally incompetent (If questionable, obtain psychiatric consult).
• A prisoner.
• An alcohol and/or drug abuser currently or recently undergoing treatment for alcohol and/or drug abuse.
• Involved with current or pending litigation regarding a spinal condition.
• Received drugs that may interfere with bone metabolism within two weeks prior to the planned date of spinal surgery (e.g., steroids or methotrexate) excluding routine perioperative anti-inflammatory drugs.
• A history of an endocrine or metabolic disorder known to affect osteogenesis (e.g., Paget's Disease, renal osteodystrophy, Ehlers- Danlos Syndrome, or osteogenesis imperfecta).
• A condition that requires post-operative medications that interfere with the stability of the implant, such as steroids. (This does not include low dose aspirin for prophylactic anticoagulation and routine perioperative anti-inflammatory drugs).
• Received treatment with an investigational therapy within 28 days prior to implantation surgery or such treatment is planned during the 16 weeks following implantation with the ZetaFuse™ Bone Graft device.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Device feasibility

Study locations

Australia · 2 centers

• Prince of Wales Private Hospital — Randwick
• Prince of Wales Public Hospital — Randwick

Identifiers

NCT: NCT05971329 · ZG-2022-003

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗