Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Spirocor
Age
30–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject with suspected S-CAD
Subject able to perform the guided breathing protocol and comply with study requirements
Subject is able and agrees to sign the informed consent form
You may not be if
Resting (supine) ECG evidence of ST-segment depression ≥ 1 mm in any lead or left bundle branch block or significant arrhythmia
Current digoxin therapy
Subject has severe valvular heart disease
Subject has congestive heart failure NYHA class III/IV
Subject has known history of myocardial infarction (ST elevation or non ST elevation)
Subject had previous coronary revascularization: CABG or PCI
Subject has pacemaker or ICD that controls sinus
Morbidly obese subject (BMI ≥ 40)
Subject has any significant medical condition which, at the investigator's discretion, may interfere with the subject's optimal participation in the study; and
Subject is currently participating in another investigational product clinical study that the investigator believes may interfere with the outcome of this study
Clareo Health | SPIROCOR Coronary Outcome by Respiratory Stress Examination
