Tivic Health ClearUP, Руководство пользователя

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9
Study 1
At the end of the study, subjects were asked
to compare their level of congestion before
treatment and ten minutes after treatment
by completing the modified nasal obstruction
symptom evaluation (NOSE) questionnaire. 59
study subjects reported moderate to severe
Clinical Study Results
3 out of 4 felt relief preferred ClearUP
The Sinus Center at Stanford University
conducted a double-blind, randomized controlled
clinical study using the ClearUP Sinus Pain Relief
device. A total of 71 subjects suffering from sinus
pain (27 subjects with chronic rhinosinusitis, 49
subjects suffering from allergic rhinitis, and 5
subjects with other sinus conditions) enrolled in
the study. 38 subjects were randomly selected to
use the ClearUP Sinus Pain Relief “active” device
and 33 subjects were randomly selected to use
the “sham” device (a device with haptic vibration
but no microcurrent stimulation). Each subject
used the active or sham device on the outside of
their sinus passages without any assistance for a
single five-minute treatment. Each subject rated
their level of pain before and ten minutes after
treatment.
Note: 24% who used the microcurrent device experienced sinus
pain reduction of 3 points or more on the visual analog pain scale
(0 no pain to 10 severe pain). Only one subject experienced minor
reddening of the skin which disappeared within minutes.
82
%
74
%