Overview

This trial is active, not recruiting.

Condition vertebral body fractures
Treatments vertebral body stenting (vbs), balloon kyphoplasty
Phase phase 4
Sponsor Synthes GmbH
Start date September 2009
End date December 2015
Trial size 100 participants
Trial identifier NCT01847898, STU-SPI-S-06-134-01

Summary

This is a randomized, controlled study to document and evaluate the clinical performance of the Vertebral Body Stenting (VBS) System in osteoporotic fractures of the thoracic and lumbar spine.

The randomized, controlled trial (RCT) will compare patients with VBS and Balloon Kyphoplasty.

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
Arm
(Experimental)
vertebral body stenting (vbs)
Vertebral Augmentation with a Stent
(Experimental)
balloon kyphoplasty
Vertebral Augmentation with a Balloon (device not specified)

Primary Outcomes

Measure
Increase and maintenance of the vertebral body height
time frame: 12 months
Visual analog scale (VAS) for back pain
time frame: 12 months
Adverse events
time frame: 12 months

Secondary Outcomes

Measure
Radiographic evaluations
time frame: 2 years
Global assessment by the patient using the VAS
time frame: 2 years
VAS leg pain
time frame: 2 years
Analgesic usage
time frame: 2 years
Neurological assessment of root tension signs, muscle strength, sensory deficit and reflexes
time frame: 2 years
Symptoms associated with position/direction of cement extrusion
time frame: 2 years
Disability using the Oswestry Disability Index (ODI)
time frame: 2 years
Quality of Life Evaluation using the EuroQol, general quality of life questionnaire (EQ-5D)
time frame: 2 years

Eligibility Criteria

Male or female participants at least 50 years old.

Inclusion Criteria: 1. Age ≥ 50 2. 1 to 3 contiguous target vertebral compression fractures (VCF) meeting the following criteria: 3. Fracture due to diagnosed or presumed underlying primary or secondary osteoporosis (Patients with AO type A1.x fractures and A3.1 fractures may be included in the study). 4. All target VCFs are between Th5 and L5 - All target VCFs to be treated show either: - Height change: An acute (< 6 month) change in VB height (>15% height loss) with height loss at the anterior, middle or posterior portion of the VB consistent with a worsening of 1 or more grades by the Genant criteria, OR - Positive MRI or bone scan: VB shows hyperintense signal on MRI-T2 or STIR sequence or target VB is positive on radionuclide bone scan - Back pain correlating with the location of at least one VCF 5. Treatment of all target VCFs is technically feasible by and clinically appropriate for BOTH vertebroplasty and balloon kyphoplasty 6. No major surgery to the spine planned for at least 1 month following enrollment 7. Pre-treatment back pain by numerical rating scale (NRS) score >= 4 (0-10 scale) 8. Subject is able to understand the risks and benefits of participating in the study and is willing to provide written informed consent 9. Psychosocially, mentally and physically able to fully comply with the protocol requirements for the duration of the study including adhering to scheduled visits, treatment plan, completing forms and other study procedures Exclusion Criteria: 1. VB morphology or configuration is such that either balloon kyphoplasty OR vertebroplasty is not technically feasible for the targeted VCFs 2. Fracture due to high-energy trauma 3. Suspected OR proven cancer inside index vertebral body. 4. Disabling back pain due to causes other than acute fracture (e.g., sacroiliac fracture, symptomatic degenerative disc disease, lumbar spinal stenosis) 5. Any painful VCF with fracture age > 6 months 6. Patients with primary tumors of the bone (e.g., osteosarcoma) or solitary plasmacytoma at site of the index VCF. Patients with these tumors in anatomic sites other than the index VCF are eligible. 7. Any objective evidence of neurologic compromise at baseline 8. Previous balloon kyphoplasty or vertebroplasty for any VCF 9. Spine stabilization beyond balloon kyphoplasty or vertebroplasty required for targeted VCFs 10. Significant clinical comorbidity that may potentially interfere with long-term data collection or follow-up (e.g., dementia, severe comorbid illness) 11. Patients requiring the use of high-dose steroid (>= 100mg prednisone or 20 mg dexamethasone per day), IV pain medication, or nerve block to control chronic back pain unrelated to index VCF(s). Patients who receive high-dose steroids for treatment of their cancer (for at least 30 days) are eligible. 12. Patients who may require allogeneic bone marrow transplantation during the course of the study 13. Spinal cord compression or canal compromise requiring decompression 14. Patients with osteoblastic tumors at the site of index VCF. Patients with osteoblastic tumors of vertebral levels not intended for kyphoplasty may be enrolled. 15. MRI contraindication (e.g. cerebral aneurysm clips, pacemaker, implanted biostimulators, cochlear implants, penile prosthesis) 16. Spinal instability as indicated by neurologic deficit, kyphosis >30°, compression >50%, translation > 4 mm, interspinous-process widening. 17. Pre-existing conditions contrary to either balloon kyphoplasty or vertebroplasty, such as: - Irreversible coagulopathy or bleeding disorder. Note regarding reversible coagulopathies: Subjects on coumadin or other anticoagulants may participate. Investigators should follow routine practices for perioperative discontinuation and re-initiation of anticoagulants. - Allergy to any device materials (e.g., bone cement) for balloon kyphoplasty or vertebroplasty. Note that in subjects with allergy to iodine-based contrast, other non-iodine contrast solutions may be used. - Any evidence of VB or systemic infection 18. Pregnant or child-bearing potential

Additional Information

Official title Study to Evaluate the Clinical Performance of the VBS System for the Treatment of Osteoporotic Vertebral Fractures in a Multicenter, Randomized, Controlled Setting
Principal investigator Paul F. Heini, Prof. Dr. med.
Trial information was received from ClinicalTrials.gov and was last updated in September 2015.
Information provided to ClinicalTrials.gov by Synthes GmbH.