I have never heard of CS helping with tinnitus but have heard of CES helping 
with tinnitus. CES (cranial electro stimulation) has been shown to help with 
tinnitus in many cases. You can buy a relatively inexpensive unit from SOTA 
called the BT7 ($175) that may help. It is part of the Bob Beck protocol which 
interestingly enough includes CS.  According to the research below CES has 
shown to be effective in over 82% cases which used the therapy. It is painless 
and actually quite pleasant and relaxing. Two electrodes attached to a headset 
sit behind the ears.The SOTA BT7 unit puts out somewhere between 4-500 
different frequencies that stimulate healing/relaxation/focus and endorphins 
which makes you feel warm fuzzies. Definately worth a try. CES is also used to 
relieve depression, anxiety, and insomnia. You haven't heard much about it 
because there is way more money in pharmaceuticals. It can be very effective 
and best of all, zero side effects. Check out braintuner.com/braintuner.htm to 
see the SOTA BT7.

Blessings
Steve  

CES Research Abstracts
  
 Engelberg, M, & Bauer, W. Transcutaneous electrical stimulation for tinnitus. 
Laryngoscope, 95(10):1,167-1,173, 1985. Presented at the Meeting of the 
Southern Section of the American Laryngological, Rhinological and Otological 
Society, New Orleans, Louisiana, January, 1985. 

At the Veterans Administration Medical Center in Cleveland, Ohio, the use of 
Alpha-Stim electrical stimulation to treat tinnitus was evaluated in a two 
experiment study. In experiment 1, 7 males, and 3 females from 23 to 69 years 
old (mean of 43 years) reported a total of 18 ears with tinnitus. Otological 
and audiological evaluations revealed all subjects except 1 had varying degrees 
of sensory hearing loss. 1 - 17 treatments of 50 µA Alpha-Stim stimulation was 
given at 0.5, 1.0, or 2.0 Hz at 13 sites around the ear for 24 seconds to 2 
minutes. The tinnitus was matched after each treatment with simulated sounds 
from a Norwest SG-1 Tinnitus Synthesizer using an ascending procedure. 6 of the 
10 subjects reported at least a 60% improvement in 8 of 18 ears, confirmed by 
tinnitus matching. 3 additional subjects (3 ears) were undecided whether 
improvement had occurred. The permanence of improvement lasted from 8 hours to 
2 months (last contact with the experimenter). 

In experiment 2, 20 subjects were divided into 2 groups, an Alpha-Stim and a 
control group, in a single blind protocol. All subjects were male, with either 
normal hearing or sensory hearing loss, most having idiopathic or noise 
exposure tinnitus. Each subject received a baseline audiological evaluation 
utilizing standard equipment referenced to ANSI standards, of air conduction, 
speech reception threshold, most comfortable loudness level, speech 
discrimination (W-22 word lists), and when indicated, bone conduction, 
impedance battery, and tone decay. The treatment was identical to experiment 1 
except the current was at 50 or 100 µA, and the stimulus duration was either 12 
or 24 seconds at the 13 sites. After each treatment the tinnitus was again 
analyzed using the same protocol. The control group had the identical procedure 
repeated twice, the first time without stimulation, followed by actual 
stimulation. Of 17 ears treated in the experimental group, 2 ears (subject 8, 
both ears) were perceived as not having improved by stimulation. Thus, 9 of 10 
subjects (90%) corresponding to 15 of 17 ears (88%) reported the stimulation as 
having improved the tinnitus. The decrease in tinnitus frequency for the 
subjective improvement ranged from 48% in subject 3 to complete remission 
(none) in the 6 ears combined for subjects 5, 7, 9, and 10. Subject 8 did not 
perceive a 19% decrease as being significant. In the control group of 15 ears, 
in only 1 ear did a subject believe there had been a change, and measurements 
indicated a 13% decrease in frequency. The range of change for the 15 ears was 
from +16 (after sham stimulation, frequency was measured as higher) to -22%. 
Once the control group had actual stimulation, 80% reported improvement in at 
least 1 ear. The measured decrease in tinnitus frequency ranged from 28% to 
complete remission (none) in 4 subjects. 

Because both groups in experiment 2 had actual stimulation, the data was 
pooled. Improvement was perceived by 20 subjects in 27 of 33 ears (82%). In 10 
cases there was complete remission. In the remaining 17 ears, the range of 
frequency decrease was from 28 to 92%. The permanence of the improvement ranged 
from 20 minutes to at least 6 months (last contact with experimentor). Most of 
the subjects had either 1 or 2 treatment sessions; however, 1 subject that had 
7 sessions found that each session tended to increase the duration of 
improvement and he concluded that he could live with his tinnitus after the 
seventh session and requested to be discharged from the program. Neither age, 
duration of tinnitus prior to stimulation, nor frequency of the tinnitus 
appeared to be a determinant to the success of treatment. Some subjects 
reported the current of 100 µA as “pins pricking” but were able to tolerate 
that amperage. Others could not tolerate greater than 50 µA. There were no 
other adverse effects reported either during or immediately following 
stimulation.

A significant number of subjects reported improvement in hearing activity but 
this could not be verified by objective evaluation. The authors concluded that 
the 82% success rate in improvement in tinnitus implies a feasible treatment 
procedure.


 

 
 


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