Human/Machine Interface: What the HeartMate 3 ® Device Tells Us About the Future

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorInternational Consortium of Circulatory Assist Clinicians

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

18 years of age or older

Scheduled Heartmate 3 ® dLVAD implantation

Disqualifiers

<18 years of age

Scheduled for dLVAD that is NOT a Heartmate 3 (R) device

Trial population

The sample for this prospective study will derive of a goal of 15 individuals recruited at each of the 10 different dLVAD implanting centers, recognizing that not all sites may be able to recruit 15 participants. Participants will be selected through sequential convenience sampling, meaning each center will recruit participants in a sequential fashion in each of the centers based upon availability.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • HeartMate 3 (R) left ventricular assist device

    Device

    No direct intervention; this is prospective study analysis of pump data from the HeartMate 3 (R) left ventricular assist device with clinical correlation to a multitude of variables and conditions we see clinically

Treatment groups

150 Participants
are divided into 7 treatment groups

7

Treatment groups

See each treatment group below.

Group A: Mayo Clinic1 intervention
Group B: University of Florida1 intervention
Group C: University of Utah1 intervention
Group D: University of California, San Francisco1 intervention
Group E: University of Chicago1 intervention
Group F: University of Kansas Medical System1 intervention
Group G: Medical University of South Carolina1 intervention

Trial outcomes

Primary outcomes

1

Survival

12-month survival post LVAD implantation stratified by percentage of abnormal pump data

Time frame
12-months

Secondary outcomes

1

Variable Correlations

Evaluate correlations and relationships between LVAD pump data (Pump parameters-Speed, Flow, PI and power; along with suction events, low flow alarms and other adventitious alarms, "PI" events, and power cable disconnects greater than 20 seconds), to demographic and clinical variables (age, gender, race, marital status, device indication, blood type, type of cardiomyopathy, height, weight, intermacs profile score, co-morbidities, vital signs, swan ganz catheter values, LVAD number values, frailty test, labs, Quality of Life testing, Cognitive, Anticoagulation Strategies, Cardiopulmonary Bypass Time, length of stay, intubation to extubation time, concommittant surgeries at implant, Temporary Support prior to implantation or following implantation, Post-surgical complications, Echocardiography results), including longitudinal pump data analyses

Time frame
12-months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

International Consortium of Circulatory Assist Clinicians

Lead sponsor

Abbott

Collaborator

Medical University of Vienna

Collaborator

Mayo Clinic

Collaborator

University of Florida

Collaborator

University of Utah

Collaborator

University of Kansas Medical Center

Collaborator

Medical University of South Carolina

Collaborator

University of Chicago

Collaborator

University of California, San Francisco

Collaborator