CHU Arnaud de Villeneuve
Montpellier, 34295, France
Location status: Recruiting
NCT Number: NCT06645990
Over the past decade, VA-ECMO has become the main mechanical support for cardiogenic shock (CS) unresponsive to medical therapy. However, recent studies failed to show any significant survival benefit at 30 days compared to medical treatment for myocardial infarction-related CS. This could be due to the complications of VA-ECMO, such as LV overload and increased LV distension, which can hinder heart recovery.
To address this, early LV unloading using devices like IABP or Impella (ECMELLA) may help by reducing LV wall stress and oxygen consumption. However, these techniques carry risks, and their benefit is still unclear. A randomized trial is needed to compare these approaches, but observational studies are also contributing to understanding the best strategies
Interested in participating?
Request Info18 year and older
All sexes
Observational
Montpellier, 34295, France
Location status: Recruiting
Over the last decade, veno-arterial extracorporeal membrane oxygenation (VA-ECMO) has become the mechanical circulatory support of choice for cardiogenic shock (CS) refractory to medical treatment. VA-ECMO allows to supplement cardiac function until myocardium recovers, or in bridge to long-term left ventricular assist device (LVAD) or to heart transplant. However, recent randomized controlled trials (RCT) and meta-analysis have failed to demonstrate any benefit of VA-ECMO in terms of 30-day survival compared with optimal medical treatment in CS related to myocardial infarction.
Reasons for these disappointing results are multifactorial. The associated risk of temporary mechanical circulatory support (t-MCS)-related complications might counterbalance any hemodynamic benefit. In addition to hemorrhagic and ischemic complications, the significant myocardial impact due to VA-ECMO drawbacks should not be overlooked. Indeed, while VA-ECMO restores systemic perfusion, it can also lead to an increase in left ventricle (LV) loading conditions. Although LV distension is not consistently observed, recent publications strongly suggest that the origin of LV overload seems to be multifactorial and contributes partially to cardiac remodeling through the modulation of cardioprotective cellular pathways, resulting in reduced cardiomyocyte apoptosis. Furthermore, peripheral VA-ECMO affects myocardial contractility and increases myocardial work (potential energy, stroke work, and pressure-volume area), particularly at native low blood flow.
Thus, cardiac recovery may be compromised and weaning from VA-ECMO delayed. This vicious cycle affects the patients overall prognosis, as delayed and possibly failure of VA-ECMO weaning and may convert the initial medical strategy of recovery towards heart transplantation or LVAD. To optimize the chance of VA-ECMO weaning, early LV unloading may be a good therapeutic option. It aims at increasing coronary flow directly and, indirectly, by improving sub-endocardial myocardial perfusion through decreasing LV wall stress and myocardial oxygen consumption. Currently, 2 techniques are mainly used, the intra-aortic balloon pump (IABP) and the microaxial flow pump as Impella device familly (ECMELLA). These invasive techniques carry risks of bleeding and thromboembolic complications, and the benefit/risk ratio of their use for myocardial recovery is not clearly established.
A few retrospective studies suggest that early left ventricular unloading during VA-ECMO could improve prognosis. In the absence of RCT, the choice of the technique (Impella or IABP) is mainly driven by center practice. A multicenter randomized clinical trial would be the best choice to address this question. However, due to the acute poor prognosis of these patients (50% of early deaths), reliable preliminary data about the expected effect size are necessary to design the most efficient clinical trial. Recent epidemiologic developments of observational studies, the emulated trials, allow a better control of immortal time bias and indication bias.
This innovative multicenter study will compare the effectiveness and safety of LV unloading by Impella (ECMELLA) versus IABP in terms of survival with myocardial recovery in patients with refractory CS
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
LV unloading with Impella (ECMELLA) before or within 24 h of ECMO initiation
LV unloading with IABP before or within 24 h of ECMO initiation
Time frame: from start of hospitalization until hospital discharge assessed up to 3 month
Hospital Survival without chronic mechanical circulatory support (LVAD) and heart transplantation.
Time frame: from start of hospitalization until hospital discharge assessed up to 3 month
In-hospital all-cause mortality
Time frame: from start of hospitalization until hospital discharge assessed up to 3 month
Arterial thromboembolic events; Hemorrhagic events (RBC transfusion); Hemolysis; Bacteremia; Infection of the device insertion site or the device itself
Time frame: from start of hospitalization until hospital discharge assessed up to 3 month
Total duration of invasive mechanical ventilation
Time frame: from start of hospitalization until hospital discharge assessed up to 3 month
Total duration of t-MCS
Time frame: from start of hospitalization until hospital discharge assessed up to 3 month
Total and in intensive care unit lenght of stay
Time frame: from start of hospitalization until hospital discharge assessed up to 3 month
Rate and % of patients with myocardial recovery, ventricular assist device or/and heart transplantation
Contact information is provided by the study sponsor or research team.
Aurore UGHETTO, MD
CONTACT
Clément DELMAS, MD, PhD
CONTACT
University Hospital, Montpellier
Other
Early Left Ventricular unLoading by Impella (ECMELLA) or Intra-aortic Balloon Pump for Cardiogenic Shock in Patients on VA-ECMO
Acronym: ELLIPSE1
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07293923
Acute Myocardial Infarction (AMI), Cardiogenic Shock
Tbilisi, Georgia
View Trial DetailsNCT07656259
Cardio Vascular Disease, Cardiogenic Pulmonary Oedema
Rochester, Minnesota, United States
View Trial DetailsNCT05699005
Anemia, Cardiogenic Shock
Lille, NORD, France
View Trial DetailsNCT06308055
Cardiogenic Shock, Cardiovascular Diseases
Aachen, North Rhine-Westphalia, Germany
View Trial Details