Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
AUM Cardiovascular, Inc.
CADence is an ECG and acoustic tool to assess coronary artery disease. This study's goal is to collect patient CADence information and compare it to the results of angiogram to determine performance: sensitivity and specificity. The CADence is not used to direct patient care. This is observational only.
Age
41–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Age \>40 years
Clinical indication for coronary angiogram
Willing and able to give informed consent
You may not be if
Body Mass Index (BMI) \<18.5 or \>40
Prior bypass surgery or coronary stenting
Presence of pacemaker/defibrillator
Presence of artificial valve
Presence of obvious cyanotic or pre-diagnosed congenital heart defect and coarctation of the aorta
Presence of murmurs, including valve lesions, ventricular septal defects and arteriovenous fistulae
Presence of moderate-severe valve disease
Left Ventricular Assist Device (LVAD)
Presence of scars on the site thorax areas
Participation in trial within 30 days prior to collecting CADence data except participation in registry studies.
Asthma or chronic obstructive pulmonary disease (COPD) with active wheezing
Inability to lie in supine position
Heart Transplant
Clareo Health | Angiographic Comparison in an Observational Study of CADence (The AMBIENCE Study)
