Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Withings
With
Syntactx
Age
22–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male or female who are 22 years of age or older,
Subject able to read, understand, and provide written informed consent,
Subject willing and able to participate in the study procedures as described in the consent form,
Subject able to communicate effectively with and willing to follow instructions from the study staff.
You may not be if
Vulnerable subject with regard to regulations in force
* Subject who is deprived of liberty by judicial, medical or administrative decision,
* Underage subject,
* Legally protected subject, or subject who is unable, linguistic or psychic incapacity, to sign the written informed consent form.
* Subject within several of the above categories,
Subject who refused to participate in the study,
Subject mentally impaired resulting in limited ability to cooperate
Subject with electrical stimulation by pacemaker
Patient with pathologic disorder that may affect motricity resulting in significant tremor that prevents subject from being able to hold still (e.g Parkinson disease)
Patient unable to stay in an upright position for the duration of study measures
Acute myocardial infarction (MI) within 90 days of screening or other cardiovascular disease that, in the opinion of the Investigator, may increase the risk to the subject or renders data uninterpretable (e.g., recent or ongoing unstable angina, decompensated heart failure, active myocarditis or pericarditis)
Acute pulmonary embolism or pulmonary infarction, within 90 days of screening
Stroke or transient ischemic attack within 90 days of screening
Active life-threatening rhythms as determined by the investigator (ventricular tachycardia, ventricular fibrillation, 3 rd -degree heart block).
History of life-threatening rhythms as determined by the investigator (ventricular tachycardia, ventricular fibrillation, 3 rd -degree heart block)
Symptomatic (or active) allergic skin reactions such as eczema, rosacea, impetigo, dermatomyositis or allergic contact dermatitis over electrode attachment sites
Known sensitivity to medical adhesives, isopropyl alcohol, or electrocardiogram (ECG) electrodes including known allergy or sensitivity to fluoroelastomer bands
