Neuromonics Launches First U.S. Clinical Study to
Assess Long-Term Tinnitus Treatment
Editor: Neuromonics is starting a clinical trial of their tinnitus
treatment program. Early research indicates significant improvement in
over 90 percent of participants. Here's the press release.
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Post-Market Study Will Add to Growing Body of Treatment Data
Neuromonics today announced the initiation of the first post-market
U.S. study, to evaluate long-term outcomes for the Neuromonics Tinnitus
Treatment. This is an FDA-cleared therapy proven to interact, interrupt
and desensitize tinnitus disturbance for long-term benefit. Unlike
traditional therapies, the Neuromonics Tinnitus Treatment comprehensively
addresses the neurological, psychological and audiological basis of
tinnitus. Patient enrollment is now underway, and the first patient has
started treatment at Silverstein Institute.
Primary endpoints for the Customized Acoustic Stimulation for Long-Term
Medical Benefit (CALM) Study include clinically significant reductions in
tinnitus disturbance and quality-of-life improvements, with patients
evaluated after six months and up to 36 months post-treatment. This
national study will include up to 10 clinical sites with a planned
enrollment of 100 moderate-to-severe tinnitus patients collectively. The
study's lead investigator, Jack Wazen, M.D., of the Silverstein Institute,
will manage and oversee the trial. The two primary sites for the study are
the Silverstein Institute in Sarasota, Fla., and the Cleveland Clinic in
Cleveland, Ohio.
Tinnitus affects as many as 50 million people in the U.S. Within this
patient population, 10 to 15 million seek medical treatment and 2 million
have severe, highly disturbing tinnitus. The Centers for Disease Control
and Prevention report 1 million new cases of tinnitus are identified each
year and 200,000 per year are severe cases. Tinnitus symptoms can be so
extreme that they negatively impact normal daily activities and could lead
to additional medical conditions, such as anxiety, depression, sleep
deprivation and elevated stress.
"The millions of patients affected by tinnitus have traditionally had
limited therapeutic options," said Dr. Wazen. "Neuromonics Tinnitus
Treatment represents the first tinnitus treatment with long-term benefit,
as demonstrated by previous studies. By leading the CALM Study, I hope to
further our understanding of how Neuromonics Tinnitus Treatment improves
quality of life and tinnitus disturbance, so that physicians and
audiologists nationwide can continue making informed decisions about its
clinical use."
"Neuromonics looks forward to expanding upon the positive outcomes that
have been seen in previous studies," said Jack Springer, director and CEO
of Neuromonics U.S.A. "Neuromonics is committed to sponsoring long-term
outcomes-based trials evaluating the therapy's lasting efficacy in this
difficult-to-treat patient population. Our goal is to prove that by
addressing the underlying neurological and psychological causes of
tinnitus, patients may experience long-term, quality-of-life
improvements."
Enrollment Information
To inquire about participating in the study, email info@neuromonics.com
or call 1-866-606-3876.
CALM Study Primary Investigator
Jack Wazen, M.D., is one of the nation's leading authorities on hearing
and balance disorders, pioneering new research in treatments for deafness,
hearing loss and other auditory complications. Prior to the Silverstein
Institute, Dr. Wazen spent 23 years as a researcher, professor and
practitioner with Columbia University and the Columbia-Presbyterian
Medical Center.
About the Neuromonics Tinnitus Treatment
Neuromonics' non-invasive, FDA-cleared device is customized to the
patient's unique hearing and tinnitus profile. It delivers a customized
neural stimulus that promotes neural plastic changes, allowing the brain
to filter and process the tinnitus. The delivery system, to carry the
neural stimulus, consists of spectrally modified customized music which
engages the brain's emotional response center, the limbic system. Research
published in the April 2007 issue of Ear & Hearing demonstrates the
Neuromonics Tinnitus Treatment offers clinically significant reduction in
tinnitus disturbance in 91 percent of treated patients. The Neuromonics
Tinnitus Treatment is the most comprehensive, long-term therapy that
targets the neurological, audiological and psychological basis of
tinnitus.
Clinically administered and monitored, the Neuromonics Tinnitus
Treatment is a proven treatment that offers significant long-term
reduction of tinnitus disturbance. The therapy is delivered via a compact,
lightweight and uniquely designed medical device. Treatment typically
occurs over a six-month period, with daily use recommended for two or more
hours per day when the tinnitus is most disturbing. The treatment can take
place during regular activities such as reading, relaxing or computer
work.
About Neuromonics
Based in Bethlehem, Pa., Neuromonics is the manufacturer and
distributor of the only FDA-cleared, patented and clinically proven
medical device designed for long-term significant relief of tinnitus. With
more than 14 years of research and development, the Neuromonics Tinnitus
Treatment has treated thousands of tinnitus sufferers worldwide.
Neuromonics' goal is to help tinnitus sufferers improve their quality of
life and overcome challenges associated with tinnitus. For more
information, go to http://www.neuromonics.com.