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A Single-Center, Parallel-Controlled Clinical Study on the Validity and Safety of Electronic Sphygmomanometers in Clinical Application

A Single-Center, Parallel-Controlled Clinical Study on the Validity and Safety of Electronic Sphygmomanometers in Clinical Application

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400088454
Enrollment
Unknown
Registered
2024-08-19
Start date
2024-08-19
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

None

Interventions

Experimental Group:None

Sponsors

Jiangsu Shengze Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Age: 14 to 85 years; 2.No participation in other clinical validations within the past week; 3.Good compliance and voluntary participation in this validation.

Exclusion criteria

Exclusion criteria: 1.Subjects with mental disorders; 2.Subjects with severe heart or liver diseases; 3.Subjects with renal failure or severe arrhythmia; 4.Participants deemed unsuitable by clinical trial personnel.

Design outcomes

Primary

MeasureTime frame
Systolic Blood Pressure,;Diastolic Blood Pressure;Pulse Rate;—

Countries

China

Contacts

Public ContactHe Chuan

Jiangsu Shengze Hospital

he-chuan@outlook.com+86 139 6210 6994

Outcome results

None listed

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