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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
ChiCTR2200063925
Enrollment
Unknown
Registered
2022-09-20
Start date
2022-09-20
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

None listed

Interventions

Experimental group:Blood pressure was measured using test instruments and control instruments

Sponsors

Hebei Chinese Medicine Hospital
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. Subjects 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
The accuracy of blood pressure value measurement;—

Secondary

MeasureTime frame
The performance evaluation of the test device;—

Countries

China

Contacts

Public ContactTan Jinchuan
1955981973@qq.com+86 13831187910

Outcome results

None listed

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