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Acute Heart Failure clinical trials

View clinical trials related to Acute Heart Failure.

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NCT ID: NCT04740242 Completed - Heart Failure Clinical Trials

Metabolic Alkalosis in Heart Failure

Start date: January 1, 2021
Phase:
Study type: Observational

Metabolic alkalosis (MA) is the most common acid-base disorder and when it's severe it can have effects on cellular function and contribute to an increase in mortality. MA is a common complication of heart failure (HF) especially when patients are treated with diuretics, but few studies have analyzed the prevalence of acid-base disorders in patients with HF. All these studies have shown that MA is more common in patients with HF in more advanced stages and that the use of diuretics increases the prevalence of MA. The study hypothesis, based on clinical experience and the few data that exist in the scientific literature, is that MA is a frequent analytical disorder in patients admitted for decompensated HF and that its presence entails a worse short-term vital prognosis. The ALCALOTIC study is an observational cohort and prospective study. The main objectives of the study are the following: 1. To determine the prevalence of MA in patients admitted for decompensated HF 2. To analyze if there are differences in patients admitted for HF according to the presence of MA on admission 3. To determine if the presence of MA has an influence on the short-term prognosis in patients admitted for decompensated HF

NCT ID: NCT04549701 Completed - Heart Failure Clinical Trials

Inferior Vena CAVA and Lung UltraSound-guided Therapy in Acute Heart Failure

CAVAL US-AHF
Start date: March 20, 2022
Phase: N/A
Study type: Interventional

Between 25% and 30% of patients hospitalized for acute heart failure (AHF) are readmitted within 90 days after discharge. Mostly due to persistent congestion on discharge. However, as the optimal evaluation of decongestion is not clearly defined, it is necessary to implement new tools to identify subclinical congestion to guide treatment.

NCT ID: NCT04252404 Completed - Acute Heart Failure Clinical Trials

FranceLEVO - Zimino Registry (FZR)

FZR
Start date: February 3, 2020
Phase:
Study type: Observational

The French National Authority for Health (Haute Autorité de santé) requested a registry study to obtain post-market surveillance data to describe baseline clinical profiles, management and outcome of patients treated with Zimino®. This study is designed to provide real-life data on the use, safety and clinical outcomes of Zimino® in routine clinical practice in France.

NCT ID: NCT04245605 Completed - Acute Heart Failure Clinical Trials

Invasive Coronary Angiography Early in Ischemic Heart Failure

ICE-HF
Start date: April 1, 2010
Phase:
Study type: Observational

To compare the outcomes of patients with acute heart failure who undergo early coronary angiography vs. usual care

NCT ID: NCT03903198 Completed - Acute Heart Failure Clinical Trials

Care Pathways of Acute Heart Failure Patients: Impact on In-hospital Mortality.

Start date: June 2014
Phase:
Study type: Observational

The investigators conducted a prospective observational study to describe the different pre-hospital and in-hospital pathways of patients with acute heart failure (AHF) and their association with in-hospital mortality.

NCT ID: NCT03806972 Completed - Acute Heart Failure Clinical Trials

Short and Long Term Prognosis of Patients Admitted to the ED With Acute Heart Failure

CRF
Start date: June 1, 2009
Phase:
Study type: Observational [Patient Registry]

Heart failure (HF) is the leading cause of hospitalization ,rehospitalization and mortality for adults over 65 years of age. This study aimed to assess mortality, and hospitalization rates at 30 days and one year after dicharge of patients with heart failure (HF) with reduced ejection fraction (HFrEF) compared to HF with preserved ejection fraction (HFpEF).

NCT ID: NCT03683212 Completed - Acute Heart Failure Clinical Trials

Early and Comprehensive Care Bundle in Elderly for Acute Heart Failure: a Stepped Wedge Cluster Randomized Trial

ELISABETH
Start date: December 10, 2018
Phase: N/A
Study type: Interventional

This is a prospective multicentre (N=15), stepped-wedge randomized trial that aims to evaluate the benefit of a protocolised comprehensive care bundle for early management of acute heart failure in the ED.

NCT ID: NCT03517514 Completed - Acute Heart Failure Clinical Trials

Heart Failure Hospital Readmissions and Physical Therapy

Start date: February 1, 2018
Phase:
Study type: Observational

This is a dissertation study which is divided into three different studies in order to answer the main research question (Study 3). The primary aim of this research (dissertation) is to investigate all-cause 30-day hospital readmission using functional mobility (5mWT, 30STS, 6MWT, TUG), psychosocial attributes (KCCQ-12, HADS, ESSI), adherence to home exercise program, participation in a supervised exercise program, and number of follow up checkups with physicians or advanced health providers of patients with Acute Decompensated Heart Failure (ADHF) diagnosis who were discharged from a tertiary teaching hospital. Study 1: What is the effect of acute physical therapy on functional ability in individuals admitted with ADHF? Study 2: What is the effect of acute physical therapy on psychosocial attributes in individuals admitted with ADHF? Study 3: Which factors such as functional mobility (5mWT, 30STS, 6MWT, TUG), psychosocial attributes (KCCQ-12, HADS, ESSI), adherence to home exercise program, participation in a supervised exercise program, and number of follow up checkups with physicians or advanced health providers predict all-cause 30-day hospital readmission in patients discharged from a tertiary, teaching hospital with ADHF diagnosis?

NCT ID: NCT03302910 Completed - Acute Heart Failure Clinical Trials

Short Stay Unit vs Hospitalization in Acute Heart Failure

SSU-AHF
Start date: December 6, 2017
Phase: N/A
Study type: Interventional

The majority of the over one million annual AHF hospitalizations originate from the emergency department. Admitting and re-admitting lower risk AHF patients who don't need prolonged hospitalization may increase their risk for poor outcomes and decrease their quality of life: Safe alternatives to hospitalization from the ED are needed. We propose a strategy-of-care, short stay unit management of AHF (i.e. less than 24 hours), will lead to improved outcomes for lower risk AHF patients.

NCT ID: NCT03243773 Completed - Acute Heart Failure Clinical Trials

Evaluation of Lung Ultrasound in Acute Heart Failure

ELUSIA
Start date: March 1, 2016
Phase:
Study type: Observational

Acute heart failure is a life threatening condition requiring rapid diagnosis and treatment. However, the differentiation between heart failure and other conditions presenting with acute dyspnea is notoriously difficult in the emergency room. Point-of-care lung ultrasound is a simple, rapid and noninvasive technique directly visualizing fluid content in the lung as evidence for acute heart failure. A number of publications showed the diagnostic utility of lung ultrasound in the diagnosis of heart failure, but many open questions remain. The goal of this study is to evaluate the diagnostic accuracy of lung ultrasound to predict a cardiac origin of dyspnea in unselected patients in the emergency room as compared to standard evaluation. Further goals are to evaluate if lung ultrasound provides additional diagnostic information as compared to clinical examination, NT-proBNP and chest X-ray, to compare the diagnostic accuracy of lung ultrasound in different patient subgroups (heart failure with preserved vs reduced ejection fraction, de novo vs decompensated chronic heart failure, age ≥75 vs <75 years, women vs men and presence vs absence of concomitant pulmonary disease) and to compare demographics and clinical characteristics in different patient populations. 300 patients, aged ≥18 years presenting to the emergency room (ER) with acute dyspnoe as principal complaint will undergo initial clinical assessment of the likely etiology of dyspnea by the ER physician in charge. The second assessment by the same physician will include results of NT-proBNP according to predefined cutoffs. Final diagnosis ("Gold Standard") will be done by two experienced investigators after patient discharge taking into account the complete medical record except the results of lung ultrasound. Assessment of chest X-ray and lung ultrasound by investigators will be preforemd blinded regarding all other results.