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Clinical Accuracy Investigation for Wrist Electronic Blood Pressure Monitor

Clinical Accuracy Investigation for Wrist Electronic Blood Pressure Monitor

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106277
Enrollment
Unknown
Registered
2025-07-21
Start date
2025-07-21
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Hypertension

Interventions

Experimental group:The selected subjects were measured non-invasively using a watch-type electronic sphygmomanometer and compared with the mean systolic and diastolic blood pressure obtained by the tw

Sponsors

Shenzhen Longgang District Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate and sign the informed consent form; 2. Age 12~85 years old, gender is not limited; 3. Patients or healthy volunteers who need to have their blood pressure checked; 4. The subject's wrist circumference (15cm~21cm) is suitable for the size of the experimental medical device.

Exclusion criteria

Exclusion criteria: 1. People with very weak Korotkoff sound and cannot judge accurately; 2. Patients with arteritis or arterial occlusive disease; 3. Pregnant people (including preeclampsia patients); 4. Diabetic patients; 5. Patients with atrial fibrillation; 6. Participated in other drug clinical trials within 30 days; 7. Subjects who are not suitable to participate in this clinical study in the opinion of the investigator.

Design outcomes

Primary

MeasureTime frame
Systolic pressure;Diastolic pressure;

Countries

China

Contacts

Public ContactGang Fu

Shenzhen Longgang District Third People's Hospital

fugangxuwei@163.com+86 153 6065 9238

Outcome results

None listed

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