Non-Invasive Detection of Right-to-Left Cardiac Shunts

NCT07420400 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2026-02-19

No results posted yet for this study

Summary

This study will test the sensitivity of a novel, battery-powered, non-invasive ultrasound device to detect a right-to-left shunt

Conditions

  • Patent Foramen Ovale (PFO)

Interventions

DIAGNOSTIC_TEST

Point-of-care ultrasound

Point-of-care ultrasound device to detect microbubbles in the intracranial circulation

Sponsors & Collaborators

  • Burl Concepts, Inc.

    collaborator INDUSTRY
  • Scripps Health

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-01-07
Primary Completion
2027-01-01
Completion
2027-03-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07420400 on ClinicalTrials.gov