desyncra for tinnitus - patient trifold

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Neurons in the auditory cortex become hyperactive and synchronized while neighboring regions display sympathetic behavior. This synchronized state is perceived by patients as tinnitus. CR ® Neuromodulation disrupts and desynchronizes hyperactivity in the brain The Desyncra for Tinnitus therapy applies CR ® Neuromodulation technology to disrupt and “desynchronize” this pathological behavior in the brain. Research has revealed how the hyperactivity behind tinnitus can be observed in the auditory cortex. The auditory cortex is physically organized according to the pitch of sounds that it perceives, from low to high pitch. The Desyncra proprietary pitchmatching procedure makes use of this to target the therapy to the hyperactive region in the auditory cortex. The Scientific SOLUTION Beyond Tinnitus CR ® Neuromodulation therapy offers solutions beyond tinnitus to other neurological pathologies, including Parkinson’s disease, epilepsy and migraine. Desyncra for Tinnitus offers a unique, scientific solution to tinnitus. The mode of delivery is quite different for each of these neurological conditions. Yet in each case, the CR ® Neuromodulation is designed to disrupt the synchronized activity and reduce the patient’s symptoms. Research Worldwide Desyncra research is global, including at Stanford University, Veterans Affairs Portland, and centers in England and Germany. Published clinical research involving hundreds of patients Discover more at desyncra.com Desyncra Inc. 1137 Pearl St #201 Boulder,CO 80302 United States Office: 720-389-0669 Toll Free: 844-444-2266 [email protected] Desyncra TM for Tinnitus has FDA clearance and carries the CE Mark. Targeting the Tinnitus Recent developments in neuroscience have led to a clearer understanding of the neural activity behind tinnitus. 1 Synchronized Partially Synchronized Desynchronized Primary Auditory Cortex Secondary Auditory Cortex Coresponds to apex of cochlea 0.5 1 2 4 8 16 Coresponds to base of cochlea 1. Tass et al. Restor Neurol Neurosci. 2012 TI16-0106_Letter_E16-00

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Neurons in the auditory cortex become hyperactive and synchronized while neighboring regions display sympathetic behavior. This synchronized state is perceived by patients as tinnitus.

CR® Neuromodulation disrupts and desynchronizes hyperactivity in the brain

The Desyncra™ for Tinnitus therapy applies CR® Neuromodulation technology to disrupt and “desynchronize” this pathological behavior in the brain.

Research has revealed how the hyperactivity behind tinnitus can be observed in the auditory cortex.

The auditory cortex is physically organized according to the pitch of sounds that it perceives, from low to high pitch.

The Desyncra™ proprietary pitchmatching procedure makes use of this to target the therapy to the hyperactive region in the auditory cortex.

The Scientific SoluTion

Beyond TinnitusCR® Neuromodulation therapy offers solutions beyond tinnitus to other neurological pathologies, including Parkinson’s disease, epilepsy and migraine.

Desyncra™ for Tinnitus offers a unique, scientific solution to tinnitus.

The mode of delivery is quite different for each of these neurological conditions. Yet in each case, the CR® Neuromodulation is designed to disrupt the synchronized activity and reduce the patient’s symptoms.

Research WorldwideDesyncra™ research is global, including at Stanford University, Veterans Affairs Portland, and centers in England and Germany.

Published clinical research involving hundreds of patients

Discover more at desyncra.comDesyncra™ Inc. 1137 Pearl St #201 Boulder,CO 80302 United States

Office: 720-389-0669 Toll Free: 844-444-2266

[email protected]

DesyncraTM for Tinnitus has FDA clearance and carries the CE Mark.

Targeting the TinnitusRecent developments in neuroscience have led to a clearer understanding of the neural activity behind tinnitus. 1

Synchronized Partially Synchronized DesynchronizedSynchronized Partially Synchronized Desynchronized

Primary Auditory Cortex

Secondary Auditory Cortex

Coresponds to apex of cochlea

0.51 2 4 8 16

Coresponds to base of cochlea

1. Tass et al. Restor Neurol Neurosci. 2012 TI16-0106_Letter_E16-00

Neurotherapy on an iPodThe Desyncra™ therapy is delivered using a customized iPod device with custom designed earphones. The thera-peutic tones are tailored to your exact tinnitus profile.

Noninvasive targeted therapy tailored to you

Comfortable and ConvenientThe therapeutic tones are quiet and yet audible, so you can continue with your everyday activities.

36 Week TherapyDesyncra™ for Tinnitus offers therapy over 36 weeks.

The therapy starts with an initial fitting appointment, and is followed by further visits at 3, 8, 12, 24 and 36 weeks.

Your audiologist will ensure that the therapeutic tones are continually optimized to the profile of your tinnitus.

Followup sessions ensure continually optimized treatment

Changed Neural BehaviorDesyncra™ for Tinnitus is designed to change the patterns in neural tinnitus networks.

Reduced tinnitus brain wave activity

Improved symptoms are reflected in EEG imaging, showing reduced delta wave activity across tinnitus neural networks.

Reduced Tinnitus SymptomsDesyncra™ for Tinnitus is a targeted therapy designed to change the patterns in your tinnitus neuronal networks and reduce the distressing symptoms, including loudness and annoyance.

Reduced loudness and annoyance

36 Weeks

A B B B B B

A B Follow-UpInitial Fitting

Duration 90 Minutes 60 Minutes

Loudness & Pitch Discrimination

Pitch Match & Programming

Diagnostic Questionnaires

Before After

Long Term ReliefTypically patients experience benefits within a few weeks of starting therapy. However, the benefits last beyond the 36 week therapy period. CR® Neuromodulation technology is applied to disrupt and “desynchronize” this pathological behavior in the brain.

Over 3,000 tinnitus patients treated

Reduced Loudness and Annoyance (VAS Scores)

Before Therapy 24 Weeks

80

70

60

50

40

30

20

n=66

62

46 46

68

Loudness Annoyance

Figure 1: Williams et al. Front Neurol. 2015

Figure 2: Adapted from Adamchic et al. Human Brain Mapping 2014