NCT04464499Active, not recruiting
Validation Study of WITHINGS BPM Core for the Detection of Atrial Fibrillation
Source: ClinicalTrials.gov · Last updated 18 Feb 2026
Brief summary (registry, in English)
The proposed clinical study aims to validate the diagnostic performance, compared to a reference ECG, of the electrocardiographic function of the BPM Core developed by Withings for the automatic identification of atrial fibrillation (AF).
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 160 (estimated)
- First submitted
- 3 Jul 2020
- Start date
- 6 Jul 2020
- Primary completion date
- 15 Mar 2021
- Lead sponsor
- Withings
- Diseases
- Atrial fibrillation
- NCT number
- NCT04464499
What you commit to
- Study type: Observational
- Planned participants: 160
- From 6 Jul 2020 to the primary completion date, 15 Mar 2021
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- Vulnerable subject with regard to regulations
- Pregnant, parturient or breastfeeding woman,
- Subject who is deprived of liberty by judicial, medical or administrative decision,
- Underage subject,
- Legally protected subject, or subject who is unable to sign the written informed consent form,
- Subject who is not beneficiary or not affiliated to a social security scheme,
- Subject within several of the above categories,
- Subject who refused to participate in the study,
- Subject in linguistic or psychic incapacity to sign a written informed consent form,
- Subject in physical incapacity to wear a blood pressure monitor
- Subject with electrical stimulation by pacemaker
- Significant tremor that prevents subject from being able to hold still
- Known sensitivity to medical adhesives, isopropyl alcohol, or ECG electrodes
Who the study is looking for
- male or female who are 18 years or older
- Subject who signed the written informed consent form,
- Able to communicate effectively with and follow instructions from the study staff
- Person with an arm circumference between 22 and 42 cm
Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| ICPC Floréale Coordinator of this site? Confirm its status | Bagnolet | France | Unknown status |
| ICPC Turin Coordinator of this site? Confirm its status | Paris | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.