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Cardiogenic Shock clinical trials

View clinical trials related to Cardiogenic Shock.

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NCT ID: NCT04775472 Completed - Cardiogenic Shock Clinical Trials

Early Left Atrial Septostomy Versus Conventional Approach After Venoarterial Extracorporeal Membrane Oxygenation

EARLY-UNLOAD
Start date: March 4, 2021
Phase: N/A
Study type: Interventional

The use of venoarterial-extracorporeal membrane oxygenation(VA-ECMO) was associated with lower in-hospital mortality in patients with cardiogenic shock. However, VA-ECMO has a deleterious effect for hemodynamics. It can increase left ventricular end-diastolic pressure(LVEDP), followed by left ventricular dilatation, abnormal opening of aortic valve and jeopardizes of myocardial recovery. Therefore, several methods have been used to reduce LVEDP. Among these, left atrial septostomy is effective, but less invasive than surgical left ventricular unloading. However, there is few data regarding this issue. Therefore, the investigators will evaluate the effect of routine, early left atrial septostomy in patients with VA-ECMO for the treatment of cardiogenic shock.

NCT ID: NCT04642768 Completed - Cardiogenic Shock Clinical Trials

Treatment With the Ketone Body 3-hydroxybutyrate in Patients With Cardiogenic Shock

KETO-SHOCK1
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Background Cardiogenic shock is a life-threatening state of acute heart failure with severely depressed blood pressure and organ perfusion. The 30-day mortality is reported as high as 50%. To date, no randomized trial has documented a survival benefit of any medical treatment in this patient group. In a first-in-man study the investigators have recently discovered that treatment with ketone bodies increases cardiac output by 2 liters per minute. Objective The present study aims to examine the direct effects of ketone body supplements on the heart function in patients hospitalized with cardiogenic shock. Also, the aim is to determine the relative need for medical circulatory support following ketone body supplement. Design A randomized double-blind cross-over study of the hemodynamic effect of enteral ketone ester versus placebo in 12 patients with cardiogenic shock Methods Right heart catheterization will be installed to monitor cardiac pressures and output. The investigators will observe heart function with transthoracic echocardiography. Blood- and urine samples will be analyzed for electrolytes, energy substrates and vasoactive substances. Organ perfusion is to be examined by renal ultrasonography and near-infrared spectroscopy for measuring cerebral and peripheral circulation. Perspectives This investigation may grant essential knowledge on ketosis in cardiogenic shock. This may lead to larger clinical trials, and hopefully a new and better treatment for patients with cardiogenic shock.

NCT ID: NCT04548739 Completed - Cardiac Arrest Clinical Trials

Cerebral Autoregulation in Pediatric ECMO (ECMOX 2)

ECMO-ECMOX2
Start date: October 22, 2020
Phase:
Study type: Observational

Children supported by Extra-Corporeal Membrane Oxygenation (ECMO) present a high risk of neurological complications and cerebral autoregulation (CA) impairment may be a risk factor. The first objective is to investigate the association between CA impairments and neurological outcome assessed by the onset of an ANE. The secondary objective is to study the underlying mechanisms influencing CA.

NCT ID: NCT04480151 Completed - Cardiogenic Shock Clinical Trials

ECLS Versus IMPELLA™ as Bridge to LVAD (ECI-BLAD)

ECI-BLAD
Start date: January 20, 2021
Phase:
Study type: Observational

In this retrospective observational multicenter study the authors tested the hypothesis that the use of IMPELLA™ pump as bridge to bridge, by giving the opportunity of active rehabilitation, should improve patient's outcomes after the implantation of Left Ventricular Assist Device (LVAD).

NCT ID: NCT04323709 Completed - Cardiogenic Shock Clinical Trials

Levosimendan for Veno-arterial ECMO Weaning

WEANECMO
Start date: January 1, 2019
Phase:
Study type: Observational

Veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is a temporary mechanical circulatory support that has been increasingly used over the last decade to restore and maintain adequate end-organ perfusion, with data suggesting improvement in outcome for patients with refractory cardiogenic shock. Nevertheless, VA-ECMO weaning should be questioned every day during patient's support. Indeed, studies have shown that the incidence of severe complications related to ECMO is associated with longer circulatory support duration. Inotropes such as dobutamine are currently used to improve myocardial contractility during VA-ECMO support with the aim to enhance left ventricular ejection, aortic valve opening and to shorten ECMO duration. However, many data suggest an increase in mortality related to predisposition to myocardial ischemia and arrythmias. Levosimendan is a calcium sensitizing inotropic agent with systemic, coronary and pulmonary vasodilatory properties and specific cardioprotective effect without increasing myocardial oxygen consumption. The use of levosimendan in patients undergoing VA-ECMO may therefore be of interest both to reduce the duration of mechanical support and to minimize severe complication with few data suggesting a potential benefit of levosimendan for VA-ECMO weaning and survival in post-cardiotomy low cardiac output syndrome with improvement of endothelial function and hemodynamics. Investigators therefore sought to investigate whether the use of levosimendan improves weaning for patients undergoing VA-ECMO support for refractory cardiogenic shock hospitalized in the surgical intensive care unit (ICU).

NCT ID: NCT04144660 Completed - Cardiogenic Shock Clinical Trials

"Treatment Use of ECMO In Pregnancy or Peripartum Patient."

Start date: October 28, 2019
Phase:
Study type: Observational

The goal of this study is to describe the use of ECMO (Extracorporeal Membrane Oxygenation) in the pregnant or peripartum patient.

NCT ID: NCT04082312 Completed - Acute Kidney Injury Clinical Trials

Acute Kidney Injury in Adult Patients Supported by VA-ECMO

AKI-ECMO
Start date: May 1, 2016
Phase:
Study type: Observational

Post-cardiotomy cardiogenic shock (PCCS) occurs in 2-6% of patients undergoing cardiac surgery, and 1% of cardiac surgery patients will require mechanical circulatory support using Veno-Arterial ExtraCorporeal Membrane Oxygenation (VA-ECMO). Acute Kidney Injury is a frequent complication in this population and negatively impacts the survival. We aimed to determine whether the timing of ECMO implantation influence the renal prognosis of these patients.

NCT ID: NCT03989531 Completed - Clinical trials for Endothelial Dysfunction

Adrecizumab in Cardiogenic Shock

ACCOST-HH
Start date: April 4, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

Cardiogenic shock is a serious medical condition with high mortality and morbidity. This trial assesses safety, tolerability and efficacy of Adrecizumab on top of standard of care in patients with cardiogenic shock.

NCT ID: NCT03910062 Completed - Cardiac Arrest Clinical Trials

Lower Limb Surveillance During VA-ECLS

Start date: April 1, 2019
Phase:
Study type: Observational

Temporary cardiac support by VA-ECLS can lead to lower limb ischemia. The aim of this study is to evaluate a multi-modal strategy (physical examination, NIRS monitoring and angiography through the reperfusion canula) of lower limb surveillance.

NCT ID: NCT03773822 Completed - Cardiogenic Shock Clinical Trials

Low Dose of Hydrocortisone and Fludrocortisone in Adult Cardiogenic Shock.

COCCA
Start date: April 19, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this randomized controlled trial is to evaluate the hemodynamic effect of low dose corticosteroid therapy (hydrocortisone and fludrocortisone) in the treatment of adult cardiogenic shock.