The use of a wristband type continuous pulse measurement device for early detection of paroxysmal atrial fibrillation: A pilot study.

The use of a wristband type continuous pulse measurement device for early detection of paroxysmal atrial fibrillation: A pilot study. - Wristband type pulse measurement for detecting paroxysmal atrial fibrillation.

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000028403

Enrollment

Registered

2017-07-27

Start date

2017-07-20

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

paroxysmal atrial fibrillation

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patient who underwent cardiac surgery. Patients of age 20 to under 90 and who consented to the trial.

Exclusion criteria

Exclusion criteria: Patients on pacemaker. Patients who are hypersensitive to rubber product. Patients with skin disease or disorder at the site of the wristband Patients who are considered unsuitable for the trial, as judged by the doctor(s) or those responsible for the safety of this trial.

Design outcomes

Primary

Measure	Time frame
The percentage at which the diagnostic result of the conventional monitoring method (central telemetric monitoring) of detecting paroxysmal atrial fibrillation matched the data obtained from the wristband device.	—

Secondary

Measure	Time frame
Incidence of paroxysmal atrial fibrillation. Sensitivity and specificity of detecting paroxysmal atrial fibrillation using the wristband device.	—

Countries

Japan

Contacts

Public ContactTomohiko Inui

Chiba University Hospital Cardiovascular surgery

nuinui5762@yahoo.co.jp09080785544

Outcome results