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Clinical trial of pulse diagnosis instrument

Clinical trial of pulse diagnosis instrument

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066358
Enrollment
Unknown
Registered
2022-12-02
Start date
2022-09-02
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulse diagnosis

Interventions

Gold Standard:SM-1A TCM four-pulse measuring instrument
Index test:Pulse diagnosis instrument

Sponsors

Guang 'anmen Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-65 years, both sexes. (2) signed the informed consent and voluntarily participated in the clinical trial.

Exclusion criteria

Exclusion criteria: (1) patients with a cardiac pacemaker. (2) unable to cooperate with the operator due to confusion, severe language or hearing impairment, mental retardation, or retardation. (3) patients who were unable to interrupt treatment for pulse diagnosis. (4) pregnant or lactating women. (5) emergency patients. (6) those diagnosed as no pulse, oblique flying pulse, or reversely closing pulse by TCM. (7) obvious scars and skin diseases on the wrist. (8) jewelry on the wrist that is difficult to take off, affects the operation, and the wrist is too thick (width over 75mm) to be put into the equipment. (9) participating in other clinical trials at the same time. (10) other conditions deemed by the investigator to be inappropriate for participation in the trial.

Design outcomes

Primary

MeasureTime frame
consistency assessment;self-repeatability assessment;

Secondary

MeasureTime frame
consistency assessment;self-repeatability assessment;

Countries

China

Contacts

Public ContactJieLi

Guang’anmen Hospital, China Academy of Chinese Medical Sciences

drjieli2007@126.com13693315418

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026