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NCT07087613Recruiting

Deep Learning Detection of Pulmonary Hypertension and Low Ejection Fraction Via Digital Stethoscope and 3-Lead ECG

Deep Learning for Detection of Pulmonary Hypertension and Reduced Left Ventricular Ejection Fraction Using a Combined Digital Stethoscope and Three-lead Electrocardiogram

Source: ClinicalTrials.gov · Last updated 18 Jun 2026

Brief summary (registry, in English)

This is a prospective, observational study evaluating whether heart sounds (phonocardiograms) and three-lead electrocardiograms (ECGs) recorded using the Eko CORE 500 digital stethoscope can help detect pulmonary hypertension (PH) and low left ventricular ejection fraction (EF ≤ 40%). PH is a condition characterized by high blood pressure in the pulmonary arteries, which can lead to heart failure and carries significant risks if undiagnosed. Low EF, which indicates reduced pumping ability of the heart, is also associated with increased risk of severe cardiac events but can remain undetected because patients often have no symptoms or only nonspecific symptoms. In this study, adults undergoing clinically indicated echocardiograms or right heart catheterization at outpatient sites will be invited to participate. Participants will complete a single study session lasting about 20 minutes, during which heart sounds and a three-lead ECG will be collected using the Eko CORE 500 device. If participants have had a clinical 12-lead ECG within 30 days of their echocardiogram or right heart catheterization, those data may also be used for analysis. A clinically indicated echocardiogram or right heart catheterization (RHC) performed within seven days before or after the Eko CORE 500 recording will serve as the reference standard to confirm the presence or absence of PH and low EF. Up to 3,850 participants may be enrolled across multiple sites to ensure that approximately 3,500 complete the study. The data collected will be used to develop and validate artificial intelligence (AI) algorithms that aim to detect PH and identify low EF, potentially enabling earlier and simpler screening for these conditions in clinical practice.

Status (registry)
Recruiting
Study type
Observational
Enrollment
3850 (estimated)
First submitted
11 Jul 2025
Start date
15 Jun 2025
Primary completion date
31 May 2027
Lead sponsor
Eko Devices, Inc.
NCT number
NCT07087613

What you commit to

  • Study type: Observational
  • Planned participants: 3850
  • From 15 Jun 2025 to the primary completion date, 31 May 2027
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients undergoing echocardiography with a limited echocardiogram (does not apply to patients undergoing right heart catheterization)

Other

  • Unwilling or unable to provide informed consent
  • Patients who are hospitalized

Who the study is looking for

  • Adults aged 18 years and older
  • Able and willing to provide informed consent
  • Completed a clinical echocardiogram or right heart catheterization within 7 days before or after study procedures

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sentara Norfolk General Hospital
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NorfolkUnited StatesRecruiting
Prairie Cardiovascular
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O'FallonUnited StatesRecruiting
St Johns Hospital, Springfield
Coordinator of this site? Confirm its status
SpringfieldUnited StatesRecruiting
Prairie Education & Research Cooperative
Coordinator of this site? Confirm its status
SpringfieldUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.