Sponsor:
Eko Devices, Inc.
Code:
NCT07087613
Conditions
Hypertension, Pulmonary
Heart Failure With Reduced Ejection Fraction
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
Eko CORE 500 Digital Stethoscope
Brief summary:
Conditions
Hypertension, Pulmonary
Heart Failure With Reduced Ejection Fraction
Study ID
NCT07087613
Start date
Jun 15, 2025
Status verified date
Jun, 2026
Completion date
May 31, 2027
Anticipated
Primary completion date
May 31, 2027
Anticipated
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Enrollment
3850 participants
Anticipated
Arms
All Participants
Interventions
Eko CORE 500 Digital Stethoscope
Primary outcome measure
Central contacts
Locations
Prairie Cardiovascular
Recruiting
O'Fallon, Illinois, United States, 62269
Contacts
Principal Investigator:
Scott Marrus, MD
Prairie Education & Research Cooperative
Recruiting
Springfield, Illinois, United States, 62769
Contacts
Principal Investigator:
Scott Marrus, MD
St Johns Hospital, Springfield
Recruiting
Springfield, Illinois, United States, 62769
Contacts
Principal Investigator:
Scott Marrus, MD
Sentara Norfolk General Hospital
Recruiting
Norfolk, Virginia, United States, 23501
Contacts
Principal Investigator:
Raymond Benza, MD
Sponsor
Eko Devices, Inc.
Last update posted
Jun 18, 2026
Last verified
Jun, 2026
Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-02. This information was provided to ClinicalTrials.gov by Eko Devices, Inc. on 2026-06-18. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.