OsseoFix™ Spinal Fracture Reduction System in Treating Spinal Compression Fracture

NCT ID: NCT00961714

Last Updated: 2022-04-28

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 15 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-08-31
• Study Completion Date: 2013-07-31

Brief Summary

The OsseoFix Spinal Fracture Reduction System facilitates the treatment of spinal fractures by providing internal fixation and stabilization using a titanium implant in conjunction with OsseoFix+™ polymethylmethacrylate (PMMA) bone cement.

The purpose of the study is to provide reasonable assurance on safety and effectiveness of the OsseoFix Spinal Fracture Reduction System for market release approval in the US.

This investigational device is intended to restore biomechanical integrity to a vertebral body that has suffered a painful compression fracture in the thoracic or lumbar spine between levels T6 and L5.

Detailed Description

This is a prospective, multi-center clinical study designed to evaluate safety and effectiveness of the OsseoFix Spinal Fracture Reduction System used with PMMA bone cement relative to the clinical expectations for treatment of vertebral compression fractures (VCFs). The study will be conducted at up to 15 investigational centers in the United States in 115 (up to 125) subjects with one or two vertebral compression fractures between levels T6 and L5 implanted with the investigational device(s).

Baseline screening will be completed to determine eligible subjects. VCFs will be confirmed by magnetic resonance imaging (MRI), or by a CT / bone scan. These diagnostic tests will be utilized to confirm that there are no retropulsed bone fragments. Subjects who meet all inclusion criteria and do not have any exclusion criteria will be scheduled to receive the OsseoFix Spinal Fracture Reduction System.

Subjects that are enrolled will be implanted with the OsseoFix Spinal Fracture Reduction System through a postero-lateral approach to the anterior vertebral body using instruments specifically designed for this procedure.

Radiographs will be taken at each follow-up visit, including baseline and post-operatively. Subject's perception of pain will be assessed using the Visual Analogue Scale (VAS). Functional outcomes will be measured using the Oswestry Disability Index (ODI) and Short Form- 36 (SF-36) questionnaires as well as their neurologic status. The VAS, ODI, SF-36 and neurologic status will be measured at baseline, 4-week, 3-month, 6-month and 12-month follow-up visits. Overall patient-satisfaction will be evaluated at all post-implant scheduled follow-up visits. Adverse event will be the recorded in all scheduled and non-scheduled visits.

The endpoint analysis will be performed and submitted when all implanted subjects have completed their 12-months follow-up.

Conditions

Vertebral Compression Fractures

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

OsseoFix

Osseofix is an titanium expandable device similar to a vascular stent that is placed in the fractured vertebral body to provide a structure in which bone cement (polymethylmethacrylate) is inserted. It is intended to be used in the thoracolumbar spine between levels T6 through L5.

Group Type: EXPERIMENTAL

OsseoFix Spinal Fracture Reduction System

Intervention Type: DEVICE

All enrolled into the study will be receiving the OsseoFix if meet inclusion / exclusion criteria.

Interventions

OsseoFix Spinal Fracture Reduction System

All enrolled into the study will be receiving the OsseoFix if meet inclusion / exclusion criteria.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• 5o years of age.
• Legal US citizen with ability to read and write.
• Acute painful fracture (≤2 months) between T6 to L5 as evidenced by plain radiography, CT / Bone scan, and/or magnetic resonance imaging.
• Subject is...

• Non-Standard Treatment:

• Inability to tolerate prolonged conservative care due to intractable pain (VAS 70/100) with maximum tolerated medication for at least 2 weeks, but less than 6 weeks; OR
• Inability to tolerate prolonged immobilization due to other comorbid conditions aggravated by immobility for at least 2 weeks, but less than 6 weeks; OR
• Intolerance of or adverse reaction to available pain medications for at least 2 weeks, but less than 6 weeks; OR
• Hospitalization secondary to pain for at least 2 weeks, but less than 6 weeks.
• Standard Treatment:

• Has undergone at least 6 weeks of conservative care.
• Have a self assessment VAS score ≥ 50 mm at the Baseline visit.
• Have 30% or greater disability score on ODI at the Baseline visit.
• Anterior wedge deformity with no less than 5% and no more than 75% loss of anterior cortical height as compared to the posterior cortical height of the same vertebral body.
• Bone mineral density (BMD) T-score of -1.5 or less, as determined by a DEXA scan.
• Intact posterior cortical vertebral body wall.
• Type A compression fractures according to AO classification of spinal vertebral fractures.
• If a transpedicular approach is utilized the pedicle diameter must be equal to or greater than 6.5 mm; however, if an extrapedicular approach is utilized there is not a minimum pedicle width requirement.
• Subject is willing and able to provide informed consent and agrees to release medical information for purposes of this study (HIPAA authorization) and to return for scheduled follow-up evaluations.

Exclusion Criteria

• Significant vertebral collapse defined as more than 75% of original vertebral height or less than 5% or a burst or pedicle fracture with posterior cortical wall disruption.
• Presence of healed fracture at the intended treatment level(s) based on a CT / bone scan or MRI.
• Compression fractures requiring treatment at 3 or more levels.
• Spinal/Foraminal canal compromised.
• Significant deformity/instability indicated by:

• Segmental kyphosis > 30 degrees, or
• translation > 4 mm.
• VAS back pain score of < 50 mm.
• ODI score of < 30%.
• Have a documented active systemic or local infection, such as AIDS, hepatitis, with a WBC greater than 11.5 and a temperature greater than 101.5°F.
• Spinal surgery in the thoracic and/or lumbar region within the past year
• Previous kyphoplasty or vertebroplasty at involved level or level above or below treated level.
• Spinal arthrodesis within 2 adjacent levels of fracture.
• Non-ambulatory prior to fracture.
• Greater than Grade 1 spondylolisthesis at level of fracture.
• Scoliosis > 10 degrees.
• BMI > 40.
• Severe cardiopulmonary deficiencies.
• Pregnant.
• Type I or II diabetes without controlled A1C level.
• Achondrogenesis disorders.
• Active malignancy, hemangiomas at the operative level(s), or multiple myeloma.
• No generally accepted medical contraindication to spinal surgery and/or general anesthesia, such as coagulopathy with a threshold for INR at 1.5 or less, and platelet count 100,000.
• A life expectancy less than the study duration or undergoing palliative care.
• Trauma injuries aside from vertebral compression fracture(s).
• Injuries that violate the posterior vertebral cortex and/or posterior column.
• Active litigation.
• Currently on workman's compensation.
• Autoimmune disorders.
• Non-spine pain that requires daily Opioids.
• Systemic long-term steroid use - greater than 6 months.
• Active multiple sclerosis or neurologic deficit caudal to fracture.
• Currently an alcohol, solvent, or drug abuser.
• Psychiatric or cognitive impairment that, in the opinion of the investigator, would interfere with the subject's ability to comply with the study requirements.
• History of allergies to any of the device components including but not limited to commercially pure titanium, titanium alloy, polymethylmethacrylate or Zirconium Oxide (ZrO2)
• Incarcerated.
• Are currently participating in another investigational study.
• Having had another device implanted in the thoracic and/or lumbar area that would interfere with the surgical approach, study device, or follow-up evaluations.

• Minimum Eligible Age: 50 Years
• Maximum Eligible Age: 105 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Alphatec Spine, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

James Yue, MD

Role: PRINCIPAL_INVESTIGATOR

Yale University

Daniel Bennett, MD

Role: PRINCIPAL_INVESTIGATOR

Integrative Treatment Centers

Locations

Scripps

La Jolla, California, United States

Boulder Neurosurgery Associates

Boulder, Colorado, United States

South Denver Neurosurgery

Littleton, Colorado, United States

Lyerly Neurosurgery

Jacksonville, Florida, United States

Southwestern Orthopedic Center

Savannah, Georgia, United States

SIU Phyysicians and Surgeons Division of Orthopaedics and Rehabilitation

Springfield, Illinois, United States

Jewish Hospital for Advanced Medicine

Louisville, Kentucky, United States

Clinical Radiology of Oklahoma

Edmond, Oklahoma, United States

NeuroSpine Institute, LLC

Eugene, Oregon, United States

Orthopaedic Associates of the Greater Lehigh Valley Easton Hospital

Easton, Pennsylvania, United States

Neurospine Solutions, PC

Bristol, Tennessee, United States

Countries

United States

Other Identifiers

08-02-A

Identifier Type: -

Identifier Source: org_study_id