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NCT05649826
Automated Ultrasound Cardiac Guidance Tool
Conditions: Ultrasound Imaging
Sex: All
Ages: 18 Years – 120 Years
Enrollment: 200
Sponsor: UltraSight
Location: United States
Summary
This research examines echocardiography images taken from cardiac patients in relation to the guidance tool developed
Eligibility Criteria
Inclusion Criteria:Males and females, aged 18 years and olderSubject willing and able to give written informed consentExclusion Criteria:Emergency (non-elective) admission within 24 h prior to participating in the studyFemale subjects who are pregnant (women of childbearing potential will provide a statement that they are not pregnant incorporated in the ICFUnable to lie as required in all the classic positions for standard TTE exam: supine on back / left decubitusSubjects who currently participate in a clinical trial, involving interventional cardiac devices.Subjects who have prior Echo exam with description of Low/Poor quality exam in the echo report.Subjects with BMI above 40.Subjects experiencing a known or suspected acute cardiac event.Subjects with severe chest wall deformity as per previous medical records and physical examination.Subjects who have undergone pneumonectomy.Subjects whose anatomy does not lend itself to yield diagnosable standard echocardiography clips (i.e., situs inversus with dextrocardia, single ventricle anatomy due to congenital heart disease, etc.).
Source: ClinicalTrials.gov (NCT05649826). StuddyBuddy aggregates publicly available trial information.