Electronic pulse reader could revolutionize sleep disorder diagnosis
NCT ID NCT07695103
First seen Jul 10, 2026 ยท Last updated Jul 10, 2026
Summary
This study explores whether a three-dimensional electronic pulse diagnostic device can accurately identify Traditional Chinese Medicine (TCM) syndromes in people with sleep disorders. Participants undergo pulse measurements and symptom assessments, and the device's results are compared with expert TCM diagnosis. The goal is to see if this technology can provide a reliable, non-invasive way to diagnose sleep disorders based on pulse patterns.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could provide an objective, non-invasive tool to help diagnose sleep disorders using Traditional Chinese Medicine principles.
- What could go wrong
- This is an early observational study with a small sample size. The device may not match expert diagnosis accurately, and results may not apply to all sleep disorder patients.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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201 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Sep 2025
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consisted of adult outpatients and inpatients with sleep disorders recruited from the Integrated Traditional Chinese and Western Medicine Hospital of Southern Medical University. Eligible participants had relatively stable symptoms, were able to complete the standardized Six-Image symptom questionnaire and electronic pulse examination, and provided written informed consent. All participants underwent expert traditional Chinese medicine syndrome differentiation and bilateral cun, guan, and chi pulse signal acquisition using the KY-M-A1 three-dimensional electronic pulse diagnostic system.
- Ages
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age between 18 and 75 years, regardless of sex. * Confirmed diagnosis of sleep disorder with relatively stable symptoms. * Ability to complete electronic pulse examination and questionnaire assessment. * Provision of written informed consent. Exclusion Criteria: * Acute phase of disease. * Severe organic cardiovascular disease, such as severe arrhythmia or heart failure. * Anatomical abnormalities of the radial artery or difficulty in pulse signal acquisition. * Pregnancy. * Other conditions considered unsuitable for pulse data acquisition by the investigators.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Integrated Traditional Chinese and Western Medicine Hospital of Southern Medical University
Guangzhou, Guangdon, 510000, China
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