atrial fibrillation
Conditions
Interventions
To wear the noninvasive pulse wave sensor, for 12 to 24 hours.
Sponsors
Tokyo Medical and Dental University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy subjects, and patients who visit Tokyo Medical and Dental University Medical Hospital for the treatment of atrial fibrillation.
Exclusion criteria
Exclusion criteria: Subjects who are not eligible for Holter electrocardiography recording
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The concordance rate between the interval of heartbeats assessed by Holter ECG and the wearable pulse wave sensor. | — |
Countries
Japan
Contacts
Public ContactTetsuo] Sasano
Tokyo Medical and Dental University Department of Cardiovascular Medicine
Outcome results
None listed