Treatment of Symptomatic Lumbar Internal Disc Disruption (IDD) With the Biostat® Disc Augmentation System: A Pilot Study

Spinal Restoration

Status

Completed

Conditions

Low Back Pain

Treatments

Biological: Biostat® Disc Augmentation System

Study type

Interventional

Funder types

Industry

Identifiers

NCT00693784

SR-BX01P-2007

Details and patient eligibility

About

The purpose of this study is to assess the safety of the Biostat Disc Augmentation System for the treatment of chronic low-back (lumbar) pain due to symptomatic internal disc disruptions (IDD) and to obtain preliminary efficacy information.

Full description

The Biostat Disc Augmentation System is a combination product combining a resorbable biologic product with a delivery device system used to prepare and insert the biologic material into a lumbar intervertebral disc.

Symptomatic IDD is defined as a painful disruption of the internal architecture of a lumbar intervertebral disc, which appears as fissures, cracks or tears within the internal structures of the disc. Pain arising from a lumbar disc may not only be perceived as pain located in the low back (axial pain), but also as somatic referred pain involving the posterior hips, buttock, lateral hips, groin, or posterior thighs.

The diagnosis of symptomatic IDD cannot currently be made on the basis of imaging studies, physical examination, or symptoms alone, and must be established with meticulously conducted disc provocation studies (provocation discography) that include pressure manometry, and identification of an adjacent normal disc.

This treatment and study are not designed for patients exhibiting other potential sources of chronic low back pain such as more advanced degenerative disc disease with significant loss of disc height (> 33%), spinal stenosis, or spondylolisthesis (see Eligibility Criteria).

Enrollment

15 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 18-75 (inclusive) and skeletally mature.
Voluntarily signs the subject informed consent form and agrees to the release of medical information for purposes of this study (HIPAA authorization).
Physically and mentally able to comply with the protocol, including ability to read and complete required forms, and willing and able to adhere to the follow-up requirements of the protocol.
Low-back pain for at least 6 months.
Pretreatment baseline low-back pain of at least 40 mm on a 100 mm visual analog scale.
Referred leg pain, if present, is of noncompressive origin and there are no clinical findings of radiculopathy.
Low-back pain is greater than leg pain (if present) as measured on a visual analog scale. If bilateral leg pain, back pain is greater than worst leg pain.
Low-back pain unresponsive to at least 6 weeks of nonoperative treatment, which may include bed rest, antiinflammatory and analgesic medications, chiropractic manipulations, acupuncture, massage, physical therapy or home-directed lumbar exercise program.
Negative response to diagnostic medial branch block or facet joint injection.
No sustained relief with epidural injection of corticosteroids.
Diagnosis of symptomatic lumbar (L1/L2-L5/S1) internal disc disruption (IDD), which requires confirmation of discogenic pain at one or two contiguous levels through positive provocation discography performed using pressure manometry and identification of an adjacent normal disc. The disc provocation studies must precisely demonstrate concordant pain (<50 psi above opening pressure) and must demonstrate a fissure(s) in the outer one-third of the posterior or lateral anulus.

Exclusion criteria

Cauda equina syndrome.
Active malignancy or tumor as source of symptoms.
Infection at the planned procedure site or active systemic infection.
Previous lumbar spine surgery.
Previous disc invasive treatment procedures at the affected level(s) (e.g., intradiscal electrothermal therapy, intradiscal radiofrequency thermocoagulation) in the past 12 months or intradiscal corticosteroid injection within the past 3 months.
Evidence of prior lumbar vertebral body fracture or trauma.
Disc bulge/protrusion at the symptomatic level(s) > 4 mm.
Presence of disc extrusion or sequestration.
Clinical findings of lumbosacral motor or sensory radiculopathy.
Leg pain is greater than low-back pain as measured on a visual analog scale.
Lumbar intervertebral foramen stenosis at the affected level(s) resulting in significant spinal nerve root compression or impingement.
Symptomatic central vertebral canal stenosis or absolute sagittal vertebral canal diameter < 9mm.
Loss of disc space height at the symptomatic level(s) greater than one-third of an adjacent normal disc (or of the expected height in the case of an L5-S1 disc).
Spondylolisthesis (≥ Grade 1) with or without spondylolysis at the symptomatic level(s).
Lumbar spondylitis or other undifferentiated spondyloarthropathy.
Dynamic instability on lumbar flexion-extension radiographs.
Positive response to diagnostic medial branch block or facet joint injection.
Positive response to diagnostic sacroiliac joint injection for those patients with pain in the sacral region
Sustained relief obtained with epidural injection of corticosteroids.
Symptomatic involvement of more than two lumbar disc levels.
Congenital or acquired coagulopathy or thrombocytopenia; or currently taking anticoagulant, antineoplastic, antiplatelet, or thrombocytopenia-inducing medications.
History of unexplained, easy, or persistent bruising or bleeding, bleeding from the gums, or bleeding problems experienced in previous surgical procedures.
Aspirin or aspirin-containing medication taken ≤7 days prior to the procedure.
Significant systemic disease, including unstable angina, autoimmune disease, rheumatoid arthritis, and muscular dystrophy.
Known or suspected hypersensitivity or allergy to drugs or components of the fibrin sealant, including aprotinin, used in the procedure.
History of, or current psychiatric condition, substance or alcohol abuse that would potentially interfere with the subject's participation in the study.
Ongoing or previous participation in another drug or device clinical study within the previous 2 months.
Subject known to be pregnant or nursing at time of enrollment or with plans to become pregnant within the planned length of follow-up (2 years).
Body habitus precludes adequate fluoroscopic visualization for the procedure or the procedure is physically impossible using the device.
Concomitant conditions requiring daily oral steroid usage for more than 30 days in the preceding 90 days.
Pending litigation against a health care professional, except where required by the insurer as a condition of coverage.
Prisoner or active military personnel who would not be available for follow-up.
Presence of ferromagnetic implants that would disallow MRI of the symptomatic disc(s).
Active or pending workers' compensation claims.