Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Verily Life Sciences LLC
Age
22–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
At least 22 years old
Able to read and speak English
Able and willing to sign written Informed Consent
Interest in participating in the study
At risk of having an AF event, as determined by having a diagnosis of paroxysmal AF (PAF) and meeting one of the following: (a) scheduled or to be scheduled to undergo AF ablation, (b) with implantable loop recorder (ILR), implantable cardioverter defibrillator (ICD), permanent pacemaker (PPM), holter monitor, or adhesive monitoring patch with documented AF burden of ≥25% in the 3 months prior to consent date, (c) CHA2DS2VASc ≥3, (d) Left atrial diameter ≥4.4 cm
Without significant limitation in ability to participate in the study, in the opinion of the investigator
You may not be if
Currently in a paced rhythm
Currently on class Ic or class III antiarrhythmic medication that has been successful in eliminating AF (no documented AF of more than 30 seconds since the initiation of the medication)
Had successful AF ablation (no documented AF of more than 30 seconds post procedure)
Known severe allergy to nickel or metal jewelry
Known allergic reaction to adhesives or hydrogels or with family history of adhesive skin allergies
Are diagnosed with persistent AF
Use of implantable neuro-stimulator
Open injury or rash where the study device or comparator will be worn
