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

Andon Health

Status: Enrolling

Conditions: Atrial Fibrillation (AF)

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT07442175

Andon Health 18

Details and patient eligibility

About

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

Enrollment: 392 estimated patients

Sex: All

Ages: 22+ years old

Volunteers: No Healthy Volunteers

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

Trial design

392 participants in 1 patient group

Subjects use Blood Pressure Monitor (TH-75) and ECG