Non-Invasive Detection of Right-to-Left Cardiac Shunts
ConditionPatent Foramen Ovale (PFO)
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorScripps Health
About this trial
This study will test the sensitivity of a novel, battery-powered, non-invasive ultrasound device to detect a right-to-left shunt
Eligibility criteria
Qualifiers
None
Disqualifiers
None
Trial design
Treatments tested in this trial
- Point-of-care ultrasound
Treatment groups
75 Participants
are divided into 1 treatment groupSponsors and collaborators
Scripps Health
Lead sponsor
Burl Concepts, Inc.
Collaborator
Source ClinicalTrials.gov