Real-World Evaluation of Eko Murmur Analysis Software in a Point of Care Setting

Terminated

• Conditions: Murmur, Heart; Innocent Murmurs; Heart Murmurs; Pathologic Murmur

• Registration Number: NCT05176899
• Lead Sponsor: Eko Devices, Inc.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-12-15
• Last Update Posted: 23 September 2024

Recruitment & Eligibility

• Status: Terminated
• Sex: All
• Target Recruitment: 103

Inclusion Criteria

Inclusion Criteria:<br><br> - Patient verbally consents to participation<br><br> - Patient is willing to have heart sounds recorded with an electronic stethoscope<br><br> - Patient is age 50 years or older<br><br>Exclusion Criteria:<br><br> - Patient is unwilling or unable to give verbal informed consent<br><br> - Patients experiencing a known or suspected acute cardiac event<br><br> - Patient is under the age of 50 years old

Exclusion Criteria

Not provided

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Impact of EMAS on echocardiogram order rates;Impact of EMAS on cardiologist consult order rates;Impact of EMAS on provider decision-making

Secondary Outcome Measures

Name	Time	Method
Impact of EMAS on patient outcomes;Sensitivity and specificity