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Heart Failure clinical trials

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NCT ID: NCT05077293 Completed - Heart Failure Clinical Trials

Building Electronic Tools To Enhance and Reinforce Cardiovascular Recommendations - Heart Failure

BETTER CARE-HF
Start date: September 9, 2021
Phase:
Study type: Observational

This is a feasibility study using a cross-over design to implement and compare a best practice alert (BPA) with an automated in-basket message to inform providers when a patient with heart failure and reduced ejection fraction (HFrEF) is not on appropriate medical therapy. The data from this pilot study will lead to a randomized controlled trial to compare the effectiveness of the BPA versus an automated in-basket message, versus usual care (no intervention).

NCT ID: NCT05072054 Recruiting - Clinical trials for Heart Failure With Reduced Ejection Fraction

Comparison of Effects of Atorvastatin Versus Rosuvastatin on Cardiac Function in Heart Failure Patients

ASTRO-CHF
Start date: October 16, 2019
Phase: Phase 4
Study type: Interventional

Statins have a protective effect in patients with established heart failure because of their lipid-lowering and pleiotropic effects. There is no randomized controlled trial comparing lipophilic versus hydrophilic statins in these patients (head to head comparison). The best evidence so far is from a meta-analysis in which the authors did an adjusted indirect comparison between lipophilic statins and rosuvastatin and found that lipophilic statins were associated with significantly lower incidence of all-cause mortality, cardiovascular mortality, and hospitalization for worsening heart failure compared to rosuvastatin (hydrophilic statin) among patients with heart failure. So, the investigators plan to conduct a randomized controlled trial comparing the effects of atorvastatin and rosuvastatin on cardiac function in patients with heart failure with reduced ejection fraction.

NCT ID: NCT05068934 Completed - Clinical trials for Heart Failure With Preserved Ejection Fraction

The Relationship Between Epicardial Fat Tissue and Cardiac Function in HFpEF Patients

Start date: October 12, 2020
Phase:
Study type: Observational

Heart failure with preserved ejection fraction (HFpEF) refers to a group of symptoms and signs of heart failure, normal or near-normal left ventricular systolic function (EF>50%), and ventricular muscle diastolic dysfunction and A clinical syndrome characterized by decreased compliance and increased stiffness. The pathogenesis of HFpEF is related to impaired lipid metabolism and inflammation. Epicardial adipose tissue (Epicardial Adipose tissue, EAT) is a kind of visceral adipose tissue. Related studies have shown that extracardiac Membrane fat is related to inflammation markers, cardiometabolic risk and cardiovascular disease.However, there is still no research investigating the the relationship between epicardial fat thickness and Cardiac Function in HFpEF patients.

NCT ID: NCT05068154 Not yet recruiting - Heart Failure Clinical Trials

Myovista vs NT Pro-BNP Heart Failure Referral Tool

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

It is hypothesised that the MyoVista wavECG has the potential to show non inferior sensitivity and specificity compared to the current heart failure pathway screening tools of BNP/NT-proBNP and 12 lead resting ECG, but has the advantage of providing a single, familiar, inexpensive point of care test which provides point of care results and can act as a prescreen, or in circumstances replacement to BNP/NTpro-BNP testing, and eliminate a proportion of the unnecessary testing and echo referrals. A comparative performance analysis of the modalities will form the basis for the study with subsequent reporting on the financial impact and societal benefits of any potential pathway change.

NCT ID: NCT05064709 Recruiting - Heart Failure Clinical Trials

Assessment of CCM in HF With Higher Ejection Fraction

AIM HIGHer
Start date: February 3, 2022
Phase: N/A
Study type: Interventional

The AIM HIGHer Clinical Trial will evaluate the safety and efficacy of Cardiac Contractility Modulation (CCM) therapy in patients with heart failure with LVEF ≥40% and ≤60%.

NCT ID: NCT05064202 Not yet recruiting - Cardiogenic Shock Clinical Trials

Unloading in Heart Failure Cardiogenic Shock

UNLOAD HF-CS
Start date: October 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this research study is to evaluate whether timely and aggressive temporary Mechanical Circulatory Support (tMCS) through the Impella 5.5® in patients with acute decompensated heart failure complicated by cardiogenic shock (ADHF-CS) has the potential to reduce the HF-CS related clinical events compared to the current standard of care.

NCT ID: NCT05063955 Recruiting - Heart Failure Clinical Trials

Mechanism of Sarcopenia in Heart Failure

MUSCLE-CHF
Start date: December 2, 2020
Phase:
Study type: Observational [Patient Registry]

The aim of the study is to provide information on the interaction between socioeconomic factors, daily physical activity, nutrition and lifestyle on loss of muscle mass and muscle function in patients with heart failure.

NCT ID: NCT05063370 Active, not recruiting - Right Heart Failure Clinical Trials

Levosimendan in Patients With Impaired Right Ventricular Function Undergoing Cardiac Surgery

Start date: August 18, 2021
Phase: Phase 2
Study type: Interventional

Perioperative right ventricular (RV) function is an important determinant of postoperative outcomes after cardiac surgery. Perioperative RV dysfunction increases the need for perioperative inotropic support, prolongs intensive care unit stay and increases in-hospital mortality, in this study, we aim to investigate the effect of the preoperative administration of levosimendan on the outcome of patients with compromised right ventricular function undergoing cardiac surgery

NCT ID: NCT05059769 Recruiting - Clinical trials for Heart Failure With Preserved Ejection Fraction

Relationship Between Ambulatory Arterial Stiffness Index and Left Ventricular Diastolic Function in Patients With HFpEF

Start date: October 10, 2020
Phase:
Study type: Observational [Patient Registry]

Heart failure with preserved ejection fraction (HFpEF) was considered as a heterogeneous disease with multi-organ and multi-system design, which is related to various complications, such as hypertension, obesity and arteriosclerosis. Ambulatory arterial stiffness index (AASI) is associated with arteriosclerosis and hypertension. There is no report on whether AASI is associated with left ventricular diastolic dysfunction in patients with HFpEF.

NCT ID: NCT05057884 Suspended - Heart Failure Clinical Trials

Breathing Exercise Against Dyspnoea in Heart Failure Patients to Improve Chemosensitivity

Breathe-HF
Start date: March 1, 2022
Phase: N/A
Study type: Interventional

An exaggerated ventilatory response (minute ventilation, V̇E) to exercise relative to exhaled carbon dioxide (V̇CO2) is common in heart failure (HF) patients with reduced as well as preserved left ventricular ejection fraction (HFrEF, HFpEF). Severity of this exaggerated response is associated with poor prognosis. This response may be triggered by pulmonary congestion and peripheral muscle myopathy. A vicious circle is fuelled by hypersensitivity of chemoreceptors to hypercapnia and sympathetic nervous hyperactivity, resulting in hyperventilation (low PaCO2). Low PaCO2 is predictive of mortality in these patients. PaCO2 can be increased acutely, e.g. by apnoea. Also, nasal breathing has been found to reduce the V̇E/V̇CO2 slope during exercise compared to oral breathing. Three previous slow breathing studies in HFrEF patients have had encouraging results with regard to reducing sympathetic activity, reflected in lowered arterial (pulmonary) blood pressure and increased EF. The investigators hypothesise that a 12-week training with nasal slow breathing followed by end-expiratory apnoea based on education, centre-based introduction and home-based 15 min/day breathing training will be effective at reducing the exaggerated ventilatory response to exercise. A total of 68 patients with stable HF seen at the HF clinics of the Inselspital (34 HFrEF, 34 HFpEF) will be randomised to the breathing intervention or usual care. Primary outcome will be V̇E/V̇CO2 slope at 12 weeks. If breathing training successfully ameliorates the exaggerated ventilatory response and perception of dyspnea during exercise, it offers an attractive tele-health based add-on therapy that may add to or even amplify the beneficial effects of exercise training.