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F1701T Blood pressure monitor clinical accuracy verification

F1701T Blood pressure monitor clinical accuracy verification

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200057308
Enrollment
Unknown
Registered
2022-03-07
Start date
2021-11-29
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

Blood Pressure

Interventions

Gold Standard:Diagnosis was performed according to ISO81060-2:2018/ AMD. 1:2020, IEC 80601-2-30:2018 and YY0670-2008 standards
Index test:Blood pressure

Sponsors

Shenzhen Hospital, University of Chinese Academy of Sciences (Guangming)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. The age of every subject should be greater than 12 years; 2. Upper arm circumference: 22-42cm.

Exclusion criteria

Exclusion criteria: 1. Heart rate abnormalities, such as atrial fibrillation,Frequent PVC, etc., resulting in large fluctuations in blood pressure and heart rate; 2. Personnel who is mentally ill and cannot submit to a clinical arrangement; 3. The pregnant or nursing women; 4. Personnel who participate in other clinical trial within 30 days; 5. Other conditions that the investigator considers inappropriate for clinical trails.

Design outcomes

Primary

MeasureTime frame
Blood pressure;

Countries

China

Contacts

Public ContactZhan Zhongqun

Shenzhen Hospital, University of Chinese Academy of Sciences (Guangming)

zzqun21@126.com+86 19925356161

Outcome results

None listed

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