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Cardiogenic Shock clinical trials

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NCT ID: NCT04682483 Recruiting - Cardiogenic Shock Clinical Trials

Cardiogenic Shock Working Group Registry

CSWG
Start date: December 4, 2017
Phase:
Study type: Observational [Patient Registry]

The Cardiogenic Shock Working Group is a multicenter registry where we collect de-identified clinical variables from the medical records and follow-up phone calls of shock patients from multiple institutions and centralize this data to a single registry for analysis of clinical outcomes.

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: NCT04478188 Not yet recruiting - Cardiogenic Shock Clinical Trials

Pressure Volume Loop

Start date: August 2020
Phase:
Study type: Observational

The investigators are doing this study and medical record review to measure simultaneous pressure and volume of the heart called pressure volumes loops before and after ventricular assist device placement for cardiogenic shock ( a severe form of heart failure). Standard of care measurements will be the sole measure of clinical determination. The investigators are measuring these PV loops to help determine which patients heart have recovered and can have the ventricular assist device removed. The investigators are also using the PV loop to indicate/correlate with certain outcomes to predict the need for LVAD patients to require additional support in the form of a right ventricular assist device. The medical record review will be performed pre-operatively, intra-operatively, and post-operatively until the day of discharge.

NCT ID: NCT04467294 Recruiting - Cardiogenic Shock Clinical Trials

Prospective Register on the Etiologies of Cardiogenic Shock and Their Prognosis at One Year.

cardiac shock
Start date: April 4, 2020
Phase:
Study type: Observational [Patient Registry]

Cardiogenic shock (CC) is one of the major challenges of current cardiology. Despite the difficulty of establishing a strict and consensual definition, it is accepted that the CC clinically corresponds to persistent hypotension (systolic blood pressure 90 mmHg for at least 30 minutes or need for vasopressor support) associated with signs of visceral hypoperfusion (confusion, mottling, oliguria, hyperlactatemia), and hemodynamic with a lowered heart index ( 1.8 L/min/m2) despite appropriate or high filling pressures. This definition of the European Society of Cardiology (ESC) masks however the great variability of hemodynamic tables grouped under the term of CC and severity levels, also variable.However, it was suggested that the etiology of CC influenced both its hemodynamic profile and therefore its therapeutic management but also its prognosis in the medium and long term.

NCT ID: NCT04451798 Recruiting - Cardiogenic Shock Clinical Trials

Acute Impact of the Impella CP Assist Device in Pts. With Cardiogenic Shock on the Patients Hemodynamic

JenaMACS
Start date: December 2016
Phase: N/A
Study type: Interventional

Prospective, monocentric open-label observational study for the assessment of acute hemodynamic effects following implantation of the IMPELLA CP cardiac support device

NCT ID: NCT04419480 Recruiting - Heart Failure Clinical Trials

Hemodynamic Monitoring to Prevent Adverse Events foLlowing cardiOgenic Shock Trial

HALO-Shock
Start date: December 31, 2020
Phase: N/A
Study type: Interventional

Pilot Prospective Randomized Unblinded Pragmatic Trial of Pulmonary Artery Hemodynamic Monitoring Following Hospitalization for Cardiogenic Shock

NCT ID: NCT04405856 Recruiting - Clinical trials for Coronary Artery Disease

Outcome of Patients Treated With IABP

Start date: February 1, 2012
Phase:
Study type: Observational

Intra-Aortic Balloon Pumps (IABP) is a widely used and effective left ventricular adjuvant therapy. IABP is an inflatable device placed in the aorta that inflates with diastole and deflates with systole. The aim of this study is to investigate the outcome of patients treated With IABP, and to evaluate the short-term and long-term outcomes of patients with IABP.

NCT ID: NCT04405817 Recruiting - Heart Failure Clinical Trials

Outcome of Patients Treated With ECLS

Start date: January 1, 2012
Phase:
Study type: Observational

Extracorporeal life support (ECLS), also called extracorporeal membrane oxygenation (ECMO), is an extracorporeal technique of providing effective circulatory and (or) respiratory failure, with a growing number of critically ill patients benefit from it. The aim of this study is to investigate the outcome of patients treated With ECMO, and to evaluate the short-term and long-term outcomes of patients with ECLS.