The purpose of this study is to validate the accuracy of the SPIROCOR System in indicating
the presence of significant coronary artery disease (S-CAD), as defined in ACC/AHA
Guidelines, in subjects with suspected S-CAD.
We will connect you to the doctor responsible for this trial and help you get more information.
Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01053975
Ages eligible for Study
30 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
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
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
Some people want to consult their doctor before considering participation in a clinical trial. This is absolutely normal as your doctor should know your medical history and should be able to advise you. If you want you can easily share the information for this trial with your doctor by clicking on the button below.