Blood Pressure Monitor (TH-75) Atrial Fibrillation Detection Function Clinical Trial

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07442175

Enrollment

392

Registered

2026-03-02

Start date

2026-02-09

Completion date

2026-07-30

Last updated

2026-03-02

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

Conditions

Atrial Fibrillation (AF)

Brief summary

This study evaluates the accuracy of a blood pressure monitor in detecting atrial fibrillation by comparing its results with a standard diagnostic method.

Interventions

None listed

Study design

Observational model

OTHER

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

22 Years to No maximum

Inclusion criteria

Atrial Fibrillation (AF): * Age ≥ 22 years; * Arm circumference between 22 cm and 42 cm; * Diagnosed with atrial fibrillation by a qualified medical institution. Non-Atrial Fibrillation: * Age ≥ 22 years; * Arm circumference between 22 cm and 42 cm; * No prior diagnosis of atrial fibrillation.

Exclusion criteria

* Pregnant women * Presence of an implanted cardiac pacemaker and/or defibrillator * Inability to cooperate with blood pressure measurement or ECG assessment * Any condition that, in the opinion of the investigator, makes the participant unsuitable for participation in this clinical study

Design outcomes

Primary

Measure	Time frame
Accuracy of atrial fibrillation detection by the TH-75 blood pressure monitor, assessed against the prespecified acceptance criteria.	Baseline

Countries

China

Contacts

CONTACTJing Li

lijing@jiuan.com022-87611660

Outcome results