Validation study of the wrist-cuff blood pressure device

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000040197

Enrollment

Unknown

Registered

2020-11-25

Start date

2020-12-01

Completion date

Unknown

Last updated

2021-01-18

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

Conditions

hypertension

Interventions

hypertension:NA

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Agree to participate in the research and to provide written informed consent and confidentiality agreement. Patient or potential patient

Exclusion criteria

Exclusion criteria: Presence of arrhythmia, heart failure, severe shock, use of heart-lung machine, vascular disease, valvular heart disease, upper extremity infection, bleeding tendency, anxiety and depression, diabetes, neurological disorders, blood clotting disorder or taking blood thinners, advanced kidney disease; Unable to use the portable data acquisition device, unable to understand the content of this study, or unwilling to participate in this study due to limb deformity of the detection part of the portable device or other reasons

Design outcomes

Primary

Measure	Time frame
Blood pressure;	—

Countries

China

Contacts

Public ContactChengyu Chen

West China Hospital, Sichuan University

chenyucheng2003@126.com+86 18980602149

Outcome results

None listed

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