Heart Failure Monitoring With Eko Electronic Stethoscopes
Stopped early
Conditions studied: Heart Failure, Crackles, Heart Failure With Preserved Ejection Fraction
In brief
This proof-of-concept study will evaluate the feasibility of the Eko DUO to measure signals relevant to heart failure (HF) decompensation, as well as the feasibility to develop an algorithm to model hemodynamic filling pressures in HF patients under active decompensation in a cardiac intensive care unit (CICU) or coronary care unit (CCU). To also assess the performance of the Eko CORE to detect signals of an HF event, this study will also take heart and lung sound measurements with the Eko CORE.
Key facts
- Study ID
- NCT04404452
- Run by
- Eko Devices, Inc.
- People needed
- 15
- Starts
- 2020-07-06
- Expected to finish
- 2020-12-14
- Last updated by the study team
- 2021-03-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults aged 18 years and older
- Patient or patient's legal healthcare proxy consents to participation
- Admitted to an CCU with a diagnosis of acute decompensated heart failure
- Presence of indwelling right heart catheter
- Receiving at least once daily hemodynamic measurements
- Willing to have heart and lung sounds recorded with two different electronic stethoscopes
You may not qualify if…
- Patient or proxy is unwilling or unable to give written informed consent
- Patient is enrolled in another study that may interfere with the observations from this study
- Acute pericarditis
- Healing chest wall wounds, such as in post-sternotomy patients
- Pacemaker (single ventricle or biventricular) with active pacing
- Mechanical ventricular support (such as ECMO, LVAD, RVAD, BiVAD, Impella, intra-aortic balloon pumps)
- Acute heart failure secondary to: a. Severe stenotic or regurgitant valvular disease; b. Acute myocardial infarction
Where it is running
- MedStar Cardiovascular Network — Washington D.C., District of Columbia, United States
Full record on ClinicalTrials.gov
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