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Human Evaluation of Overall Effectiveness for Arm-type Fully Automatic Digital Blood Pressure Monitor (ISO)

Human Evaluation of Overall Effectiveness for Arm-type Fully Automatic Digital Blood Pressure Monitor (ISO)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060531
Enrollment
Unknown
Registered
2022-06-04
Start date
2022-05-26
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Blood pressure

Interventions

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 12 years old, gender is not limited; 2. Voluntary participation in blood pressure measurement and signing the informed consent; 3. Subject could communicate well with the research doctor, and have good compliance to follow the clinical research requirements.

Exclusion criteria

Exclusion criteria: 1. Allergies of blood pressure cuffs; 2. Serious arrhythmia; 3. Pregnant women and lactating women; 4. Take other clinical trials; 5. The researchers believe that other reasons are not suitable for the subjects in this clinical study, such as consciousness disorder, and mental disorders unable to communicate informed consent.

Design outcomes

Primary

MeasureTime frame
The accuracy of Blood Pressure value measurement;

Secondary

MeasureTime frame
The performance evaluation of the test device;

Countries

China

Contacts

Public ContactGang Li

Hebei General Hospital

936770315@qq.com+86 18131121932

Outcome results

None listed

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