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Evaluation of the overall effectiveness of arm-mounted electronic sphygmomanometers

Evaluation of the overall effectiveness of arm-mounted electronic sphygmomanometers

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300076597
Enrollment
Unknown
Registered
2023-10-12
Start date
2023-10-12
Completion date
Unknown
Last updated
2023-10-16

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 People's Hospital of Hangzhou
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Pregnant woman, gestational week = 13 weeks; 2) Arm circumference of 22~42cm (including the threshold); 3) Voluntarily participate in blood pressure measurement and sign the informed consent form; 4) Able to communicate well with the study doctor, good compliance, and can follow the requirements of the clinical study.

Exclusion criteria

Exclusion criteria: 1) allergy to blood pressure cuff material; 2) severe cardiac arrhythmia; 3) other reasons, in the opinion of the investigator, that make them unsuitable for this clinical trial.

Design outcomes

Primary

MeasureTime frame
Blood pressure measurement accuracy;

Secondary

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

Countries

China

Contacts

Public ContactHongbo Zhai

The First People's Hospital of Hangzhou

zhaihb@126.com+86 139 5814 0675

Outcome results

None listed

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