RecruitingNCT05649826
Automated Ultrasound Cardiac Guidance Tool
Optimization of an Ultrasound Cardiac Guidance Tool
Sponsor
UltraSight
Enrollment
200 participants
Start Date
Feb 1, 2023
Study Type
OBSERVATIONAL
Conditions
Summary
This research examines echocardiography images taken from cardiac patients in relation to the guidance tool developed
Eligibility
Min Age: 18 YearsMax Age: 120 Years
Inclusion Criteria2
- Males and females, aged 18 years and older
- Subject willing and able to give written informed consent
Exclusion Criteria10
- 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.
- 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.).
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Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05649826