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Automated Ultrasound Cardiac Guidance Tool
RecruitingObservational study
Optimization of an Ultrasound Cardiac Guidance Tool
Who can join
Ages 18 to 120 · All sexes
Full eligibility criteria
Inclusion Criteria: 1. Males and females, aged 18 years and older 2. Subject willing and able to give written informed consent Exclusion Criteria: 1. Emergency (non-elective) admission within 24 h prior to participating in the study 2. Female subjects who are pregnant (women of childbearing potential will provide a statement that they are not pregnant incorporated in the ICF 3. Unable to lie as required in all the classic positions for standard TTE exam: supine on back / left decubitus 4. Subjects who currently participate in a clinical trial, involving interventional cardiac devices. 5. Subjects who have prior Echo exam with description of Low/Poor quality exam in the echo report. 6. Subjects with BMI above 40. 7. Subjects experiencing a known or suspected acute cardiac event. 8. Subjects with severe chest wall deformity as per previous medical records and physical examination. 9. Subjects who have undergone pneumonectomy. 10. 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.).
About the study
This research examines echocardiography images taken from cardiac patients in relation to the guidance tool developed
Sponsor: UltraSight · Participants: 200 · Started: Feb 1, 2023
Contact the study team
- Robert Ehrman, MD · Phone: 313-5771268
- Laura Gowland, Sonographer · Phone: 313-5771268
Official record on ClinicalTrials.gov — NCT05649826
Locations in the U.S.
| Michigan | Wayne University, Detroit |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.