Spine Patient Society Partners with SpineMark (Clinical Trials with Disc Replacement and Motion Preservation)

[Justin]

The Spine Patient Society is excited to announce our new partner, the SpineMark Corporation. :thumpup:

SpineMark Corporation is dedicated to providing patients with centralized access to comprehensive spine services.

By building a global network of spine Research Centers, Centers of Excellence and state-of-the-art medical conference facilities, SpineMark is “helping to transform the standard of spine care” for patients afflicted with spine disorders and injuries. www.spinemark.com

Here's a link to SpineMark's website. Make sure to click on the tab entitled "Featured Clinical Trials."

SpineMark Research Network: Surgical and Non Surgical Care for Cervical, Lumbar and Thoracic Spinal Disorders

[KBear]

Spine Mark is the research company in Texas Back Institute in Plano that does my follow up for my study. They are all really nice people, from my experience.

[Justin]

Spine Mark is the research company in Texas Back Institute in Plano that does my follow up for my study. They are all really nice people, from my experience.

Kathy, thanks for the information above. SpineMark's ability to connect Spine Patients with cutting edge Clinical Trials and interventions is a priceless resource.

Keep up the great work SpineMark!

[Justin]

Featured Clinical Research Trials

Applied Spine Technologies
Dynamic Stabilization for Lumbar Spinal Stenosis With Stabilimax NZ® Dynamic Spine Stabilization System
The purpose of this trial is to assess whether the Stabilimax NZ® is at least as safe and effective as the control therapy of fusion in patients receiving decompression surgery for the treatment of clinically symptomatic spinal stenosis at one or two contiguous vertebral levels from L1-S1. Safety and effectiveness will be assessed by means of primary study endpoints which address improvements in pain and function in the absence of major device related complications. The study hypothesis criteria for demonstrating safety and efficacy requires scientific evidence that patients classified as satisfying the primary study endpoint post device implantation is at least as good for Stabilimax NZ® recipients as that for patients undergoing fusion with posterior pedicle screw instrumentation at the 24 month followup assessment.
Stabilimax NZ

AxioMed Spine Corporation
Freedom Lumbar Disc in the Treatment of Lumbar Degenerative Disc Disease (FLD)
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
Welcome to AxioMed Spine Corporation

• Degenerative Disc Disease (DDD)

Vertiflex, Incorporated
Investigating Superion™ In Spinal Stenosis [ISISS]
The proposed prospective, multi-center, randomized clinical trial is designed to evaluate the safety and effectiveness of the Superion™ ISS compared to the X-STOP® IPD® device in healthy adults suffering from at least 6 months of moderate spinal stenosis symptoms who have been unresponsive to conservative care.

• Lumbar Spinal Stenosis
• Neurogenic Intermittent Claudication

For more information, visit SpineMark's website.