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Evaluation of overall effectiveness for Wrist Fully Automatic Digital Blood Pressure Monitor

Evaluation of overall effectiveness for Wrist Fully Automatic Digital Blood Pressure Monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069428
Enrollment
Unknown
Registered
2023-03-16
Start date
2023-03-16
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

blood pressure

Interventions

Wrist electronic sphygmomanometer group:N/A
Desktop sphygmomanometer group:N/A

Sponsors

The Ninth People's Hospital of Suzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: 1. Allergies to blood pressure cuffs; 2. Serious arrhythmia; 3. Impaired consciousness, unable to fully inform; 4. Researchers believe that other reasons are not suitable for this in this study clinical trial.

Design outcomes

Primary

MeasureTime frame
Accuracy of blood pressure measurement;Instrument performance evaluation;

Secondary

MeasureTime frame
Operation satisfaction;Pulse rate measurement accuracy;Working stability;Performance failure;Device defect;

Countries

China

Contacts

Public ContactYing Jin

Suzhou Ninth People's Hospital

sunny13211@sina.com+86 13375163966

Outcome results

None listed

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