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Clinical Test of the overall effectiveness of Arm Electronic Sphygmomanometer

Clinical verification of the overall effectiveness of arm electronic sphygmomanometer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077896
Enrollment
Unknown
Registered
2023-11-23
Start date
2022-04-28
Completion date
Unknown
Last updated
2023-11-27

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

Conditions

blood pressure

Interventions

Sponsors

People's Hospital of Hebei Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Age 12 and above, no gender limitation; 2) Voluntarily participate in blood pressure measurement and sign the informed consent; 3) Be able to communicate well with the clinical research physician, have good compliance, and follow the requirements of the clinical research.

Exclusion criteria

Exclusion criteria: 1) Those allergic to cuff material; 2) Those with severe arrhythmia; 3) Pregnant and lactating women; 4) Those participating in other clinical studies; 5) Other reasons that the investigator considers the person is not eligible for the research, such as inability to communicate informed consent due to disturbance of consciousness or mental disorder.

Design outcomes

Primary

MeasureTime frame
Accuracy of blood pressure measurement;

Secondary

MeasureTime frame
Accuracy of pulse rate measurement, convenience of product operation, and stability of work;

Countries

China

Contacts

Public ContactGang Li

Hebei Provincial People's Hospital

936770315@qq.com+86 181 3112 1932

Outcome results

None listed

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