What this means
Researchers plan to track pump data from HeartMate 3 heart devices over time and compare it with health and daily life. This is a trial that has not reported results, so it does not yet show whether the data helps.
Plain-English summary written by an AI model from the registry listing.
- Status
- Recruiting
- Who can join
- Ages 18–100
- Where
- 7 sites, including California, Florida, Illinois
The science
- Registered title
- Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future
- Trial ID
- NCT06039176 ↗
- Phase
- Not applicable
- Study type
- observational
- Conditions
- LVAD, Frailty, GI Bleed, Right Heart Failure, Infections, Hypertension, Arrhythmias, Stroke
- What is tested
- HeartMate 3 (R) left ventricular assist device
- Sponsor
- International Consortium of Circulatory Assist Clinicians
- Ages
- 18 Years to 100 Years
- Dates
- First posted Sep 15, 2023 · updated Dec 16, 2025
Registry summary
Durable left ventricular assist devices (dLVAD) have been increasingly utilized since the mid to late 1990s, with an uptick of utility starting in 2010 following expanded indications for therapy to not only include a bridge to transplantation strategy, but also for those individuals who suffer from advanced heart failure (HF) and do not qualify for cardiac transplantation. Despite the decreasing size of the newest generation devices leading to a lessened occurrence of adverse events, bleeding and infection still remain a concern for clinicians, as well as a general lack of predictability towards adverse events in individuals with a dLVAD in place. There is a lack of description in the literature currently, regarding the interface between what the pump data provides and what is seen in clinical practice. There also is little known about the effects of what is provided in the pump data, in correlation to quality-of-life following dLVAD implantation.
Therefore, the purpose of this study is to prospectively analyze normal and abnormal pump data through pump operations such as suction events, low flow alarms as well as other adventitious alarms, PI events and power cable disconnects greater than 20 seconds, from the HeartMate 3 ® dLVAD in order to clinically correlate this data to quality of life, frailty and other various medical conditions and adverse events as defined by the Interagency Registry for Mechanically Assisted Circulatory Support (Intermacs). This will be achieved through two aims: 1) Evaluate the effectiveness of dLVAD pump operations data on clinical practice application (quality of life, frailty and various medical conditions, and adverse events such as GIB, RHF, infection, hypertension, arrhythmias and stroke); and 2) Evaluate correlations and relationships of longitudinal normal and abnormal dLVAD pump operations data, to demographic and clinical variables. This study is the first study to evaluate HeartMate 3 ® dLVAD pump operations data over time for effectiveness in the clinical practice.
Sites (7)
- UCSF, San Francisco, California, United States
- University of Florida, Gainesville, Florida, United States
- University of Chicago, Chicago, Illinois, United States
- University of Kansas Medical Center, Kansas City, Kansas, United States
- Mayo Clinic-Rochester, Rochester, Minnesota, United States
- MUSC, Charleston, South Carolina, United States
- University of Utah, Salt Lake City, Utah, United States
More aging trials in these states
California · Florida · Illinois · Kansas · Minnesota · South Carolina · Utah
