About this trial
This research examines echocardiography images taken from cardiac patients in relation to the guidance tool developed
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Males and females, aged 18 years and older
Subject willing and able to give written informed consent
Disqualifiers
Emergency (non-elective) admission within 24 h prior to participating in the study
Female subjects who are pregnant (women of childbearing potential will provide a statement that they are not pregnant incorporated in the ICF
Unable to lie as required in all the classic positions for standard TTE exam: supine on back / left decubitus
Subjects who currently participate in a clinical trial, involving interventional cardiac devices.
Trial population
Up to 200 subjects will be enrolled in this study, at least 35% females and 35% males.
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Acquisition of transthoracic echocardiography media from up to 200 subjects
Several echocardiography views will be acquired from the participants, with in several acoustic windows and views