Trials / Completed
CompletedNCT05266235
Clinical Validation of the Withings ECG Monitor for the Detection of Atrial Fibrillation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 274 (actual)
- Sponsor
- Withings · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The aim of the study is to demonstrate the performance of Withings WBS08 in the automatic identification of atrial fibrillation and sinus rhythm.
Detailed description
Patients included will be those presenting for consultation in the various participating clinical services. For each patient, an ECG will be recorded with the WBS08 and with the reference device Cardiovit FT1, at rest and after an exercise session.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Validation of the Withings bodyscan scale WBS08 | Participants will undergo simultaneous recordings of ECGs with the comparator and the study device |
Timeline
- Start date
- 2022-04-14
- Primary completion
- 2022-07-28
- Completion
- 2022-07-28
- First posted
- 2022-03-04
- Last updated
- 2023-03-28
Locations
4 sites across 2 countries: Belgium, France
Source: ClinicalTrials.gov record NCT05266235. Inclusion in this directory is not an endorsement.