Electronic pulse reader could revolutionize sleep disorder diagnosis

NCT ID NCT07695103

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Not yet recruiting
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Paused for now. It may or may not start again.
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The trial has finished. Results may not be published yet.
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Cancelled before anyone took part.

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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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

201 people

The number who actually took part.

Started

Jan 2025

Finished

Sep 2025

Lead sponsor

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

18 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

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

  • Integrated Traditional Chinese and Western Medicine Hospital of Southern Medical University

    Guangzhou, Guangdon, 510000, China

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