Non-significant risk device study to conduct evaluation of the performance of new device for monitoring of cardiac function (based on previous iterations 510(k) 173156)
Age
22–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Ability to provide written informed consent
22 years of age or older
Referred for cardiac catheterization for reasons including heart failure, evaluation before transplant, pulmonary hypertension, shortness of breath, valvular disease, etc.
You may not be if
Previous Heart Transplant
Presence of Left Ventricular Assist Device
Presence of a Holter monitor or any other electrical leads on the chest at the time of sensor placement
Surgical scars/wounds/bandages/ports at the site of sensor placement
Clareo Health | Cardiac Performance System Data Collection Study
