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Clinical Trial to Evaluate the Overall Effectiveness of an Arm-Mounted Electronic Sphygmomanometer

Clinical Trial to Evaluate the Overall Effectiveness of an Arm-Mounted Electronic Sphygmomanometer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082285
Enrollment
Unknown
Registered
2024-03-26
Start date
2024-04-08
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

blood pressure

Interventions

Sponsors

The First Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age > 12 years old, gender is not limited; 2) Voluntarily participate in blood pressure measurement and sign an informed consent form; 3) Able to communicate well with the study physicians and have good compliance to follow the requirements of the clinical study.

Exclusion criteria

Exclusion criteria: 1) Hypersensitivity to blood pressure cuff materials; 2) Persons with severe cardiac arrhythmias; 3) Persons with impaired consciousness who are unable to give adequate information; 4) Others who, in the opinion of the investigator, should not participate in this study.

Design outcomes

Primary

MeasureTime frame
Blood pressure measurement accuracy;

Secondary

MeasureTime frame
Accuracy of pulse rate measurement;Evaluation of instrument performance;Instrument defects;

Countries

China

Contacts

Public ContactGuiqi Wang

The First Hospital of Hebei Medical University

wangguiqi2011@126.com+86 186 3388 9761

Outcome results

None listed

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