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Evaluation of overall effectiveness for Arm-type Fully Automatic Digital Blood Pressure Monitor(ISO)

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
ChiCTR2200063805
Enrollment
Unknown
Registered
2022-09-16
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

blood pressure

Interventions

Case group:Blood pressure measurement

Sponsors

Suzhou Science & Technology Town Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age>=12 years, regardless of gender; 2. Voluntarily participate in blood pressure measurement and sign an informed consent form; 3. Able to communicate well with research doctors, have good compliance, and can follow the requirements of clinical research.

Exclusion criteria

Exclusion criteria: 1. Allergies to blood pressure cuff materials; 2. Severe arrhythmia; 3. Individuals with consciousness disorders who cannot be fully informed; 4. The researcher believes that others are not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
The accuracy of Blood Pressure value measurement;—

Countries

China

Contacts

Public ContactGuocun Hou
ke.zhou@care-real.com+86 19951296331

Outcome results

None listed

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