M6-C artificial disc

Status: This trial has been completed.

Introduction

DISC is one of 12 sites in US, only in AZ where patients have access to the M6-C Artificial Disc: FDA IDE Pivotal Study.  If you are a patient who is interested in participating in this study, please contact DISC directly. 

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Disc on Channel 3

Status: This trial is now full.

Do you have chronic low back pain? Does your low back pain keep you from enjoying everyday life?

Low Back Pain Research Study
Desert Institute for Spine Care is conducting a research study of an investigational, one-hour procedure designed to treat chronic low back pain at its source.

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Coflex

Status: This trial is now full.

UPDATE: FDA Approved!  

Dr. Anthony Yeung, Principal Investigator in the study, along with investigators Dr. Christopher Yeung and Dr. Justin Field, participated in this clinical trial that led to this FDA approval. DISC, the only site in Arizona involved in this trial, was in the top 5 sites whose data was used for papers presented to national and international meetings authored by Josh Auerbach.

For more information, go to:
“COFLEX® INTERLAMINAR TECHNOLOGY RECEIVES FDA APPROVAL!” »
or Read on PubMed »

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CERVICORE™ INTERVERTEBRAL DISC

Status: This trial has been completed.

Introduction
The study is a multi-center, prospective, randomized controlled clinical trial that will compare the safety and effectiveness of the CerviCore™ Intervertebral Disc to anterior cervical discectomy and fusion (ACDF) with a rigid plate for radicular symptoms associated with loss of disc height, disc/osteophyte complex, or herniated disc at a single cervical spine level. The trade name of the investigational device is: CerviCore™ Intervertebral Disc.

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FlexiCore™ Intervertebral Disc Clinical Trial

Status: This trial has now been completed.

Desert Institute for Spine Care has been selected to participate in the FlexiCore™ Intervertebral Disc Study.

FlexiCore™ Intervertebral Disc Study Summary
This is a multi-center, prospective, randomized, controlled study comparing the safety and effectiveness of the FlexiCore™ Intervertebral Disc to spinal fusion surgery for the treatment of pain associated with degenerative disc disease (DDD) at a single level in the lumbo-sacral spine (L1-S1).

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Wallis Stabilization System

Status: The Wallis Stabilization Trial has now been completed.

Desert Institute for Spine Care has been selected to participate in the Wallis Stabilization System Clinical Trial.

Introduction to the Wallis Stabilization System
The Wallis Normalization System is a non-fusion, spinal stabilization device that is currently limited by US law to investigational use within the US. The Wallis clinical study is a multi-center, prospective, randomized study comparing the safety and effectiveness of the Wallis device to the latest non-surgical treatment regimen including medication, physical therapy and spinal injections. The Wallis System is designed to help with the pain caused by degenerative disc disease (DDD) by stabilizing the lumbar spine without a fusion procedure.

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Note: This trial has now been completed.

Desert Institute for Spine Care has been selected to participate in the DASCOR™ disc nucleus replacement pilot clinical study.

Study objectives for the DASCOR™ Disc Arthroplasty System pilot clinical study
This pilot clinical study is designed to evaluate the initial safety and effectiveness of the DASCOR™ Disc Arthroplasty device in subjects with single-level degenerative disc disease (DDD) of the lumbar spine from L2 to the sacrum and to provide data for use in hypothesis and endpoint determination for the pivotal study.

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Phoenix

1635 East Myrtle Avenue, Suite 400
Phoenix, AZ 85020

East Valley

3487 S. Mercy Road
Gilbert, AZ 85297

Scottsdale

8630 E. Via de Ventura, Suite 210
Scottsdale, AZ 85258

LEADERS IN MINIMALLY INVASIVE SPINE CARE
Copyright © 1996-2018 by Anthony T. Yeung, M.D., P.C.
1635 E. Myrtle • Suite 400 • Phoenix, AZ 85020 • 602-944-2900