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Age: 22Years +
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ID07442175

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

Led by Andon Health Co., Ltd · Updated on 2026-03-02

392

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

A

Andon Health Co., Ltd

Lead Sponsor

F

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating how accurately the TH-75 blood pressure monitor detects atrial fibrillation AF by comparing its results to a standard diagnostic method. The study aims to determine if this device meets specific criteria for detecting AF in adults with and without the condition. This observational research is sponsored by Andon Health Co., Ltd and focuses on adults aged 22 years and older. Participants will use the TH-75 blood pressure monitor alongside electrocardiogram ECG tests to monitor heart rhythm. The study involves measuring arm circumference to ensure proper device fit, requiring participants to have an arm circumference between 22 cm and 42 cm. Both those diagnosed with atrial fibrillation and those without will be observed during the study period. Throughout the study, researchers will compare the blood pressure monitors detection accuracy against standard ECG results. Participants will undergo blood pressure measurements and ECG assessments as part of the evaluation. The primary outcome is the accuracy of atrial fibrillation detection by the TH-75 monitor, measured against predetermined acceptance criteria. The study is expected to complete by July 30, 2026.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 22Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 22 years or older
  • Arm circumference between 22 cm and 42 cm
  • Diagnosed with atrial fibrillation by a qualified medical institution OR no prior diagnosis of atrial fibrillation
Not Eligible

You will not qualify if you...

  • Pregnant women
  • Presence of an implanted cardiac pacemaker and/or defibrillator
  • Inability to cooperate with blood pressure measurement or ECG assessment
  • Any condition making the participant unsuitable for this clinical study as judged by the investigator

Research Team

J

Jing Li

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