Automated Ultrasound Cardiac Guidance Tool
Recruiting now
Conditions studied: Ultrasound Imaging
In brief
This research examines echocardiography images taken from cardiac patients in relation to the guidance tool developed
Key facts
- Study ID
- NCT05649826
- Run by
- UltraSight
- People needed
- 200
- Starts
- 2023-02-01
- Expected to finish
- 2027-05-01
- Last updated by the study team
- 2024-05-21
Who can join
Age: 18 and older, up to 120. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males and females, aged 18 years and older
- Subject willing and able to give written informed consent
You may not qualify if…
- 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.).
Where it is running
- Wayne University — Detroit, Michigan, United States (enrolling)
Full record on ClinicalTrials.gov
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