Fibricheck Detection cApabilities for Atrial Fibrillation
Completed · Not applicable
Conditions studied: Atrial Fibrillation
In brief
Evaluation of accuracy of the FibriCheck Mobile Application on various smartphone devices, compared to the reference diagnosis.
Key facts
- Study ID
- NCT06282380
- Run by
- Qompium NV
- People needed
- 330
- Starts
- 2024-02-26
- Expected to finish
- 2024-06-26
- Last updated by the study team
- 2024-06-27
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- At least 22 years old;
- Capable of independently performing FibriCheck recordings (researcher-observed);
- Cardiology patients, hospitalized/in-clinic or consulting the cardiac outpatient clinic, with or without a diagnosis of atrial fibrillation.
You may not qualify if…
- Individuals with cardiac pacemakers, implantable cardioverter-defibrillators, or other implanted electronic devices as these can influence the natural heart rhythm;
- Individuals enrolled in another clinical trial;
- Individuals with physical or medical characteristics that prevent them from successfully taking a measurement e.g. extreme callus (i.e., rough or thickened area of skin fingertip), tremor, cognitive impairment, Parkinson's disease;
- Pregnant and/or nursing women.
Where it is running
- Northwestern Medicin — Chicago, Illinois, United States
- New York Presebyterian Queens — New York, New York, United States
- OU Medicine College — Oklahoma City, Oklahoma, United States
- University Hospital Antwerp — Antwerp, Belgium
- Ziekenhuis Oost-Limburg — Genk, Belgium
Full record on ClinicalTrials.gov
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