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Heart Failure clinical trials

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NCT ID: NCT04391491 Completed - Clinical trials for Pulmonary Hypertension

Neuregulin-1 in Patient With Different Forms of Cardiovascular Diseases: a Pilot Study

NRG-1-CVDs
Start date: March 1, 2019
Phase:
Study type: Observational

This is an observational study of Neuregulin-1 (NRG-1) plasma levels in patients with different forms of cardiovascular disease including microvascular angina (MVA), heart failure with preserved ejection fraction (HFpEF), as well as, heart failure with reduced ejection fraction (HFrEF) and pulmonary hypertension (PH). Investigators intend to identify cardiovascular diseases which are characterized by increased circulating NRG-1, considered to be a biomarker of therapeutic potential of NRG-1. Participants will undergo blood sampling over 3 days following randomisation. Patients demographics and clinical characteristics will be recorded and their associations with NRG-1 will be analysed.

NCT ID: NCT04391439 Completed - Hypertension Clinical Trials

Heart Rhythm After Intravenous Methylprednisolone Administration

Start date: January 1, 2011
Phase:
Study type: Observational

High doses of intravenous (iv.) glucocorticoids (GCs) are commonly used as a treatment for many autoimmune and inflammatory disorders. According to the European Group on Graves' Orbitopathy (EUGOGO) guidelines, intravenous methylprednisolone (IVMP) is an accepted first-line agent for active, moderate-to-severe and very severe Graves' orbitopathy (GO). This treatment is proven to be more efficient and safer than oral GCs. However, some patients may experience adverse cardiovascular effects during the administration of iv. GCs, which in rare cases may even be fatal. There are limited data, mostly obtained from case reports, reporting the occurrence of cardiac arrhythmias, acute myocardial infarction or heart failure. Increased heart rhythm (HR) has drawn attention of researchers as a possible adverse effect correlated with IVMP. During this study, investigators performed 72-hours of Holter ECG and ambulatory blood pressure monitoring (ABPM) to evaluate the impact of IVMP on patients with moderate-to-severe GO, concerning HR and blood pressure (BP) changes. In order to elucidate possible mechanism of observed changes, researchers investigated the level of potassium in serum and urine and catecholamines (epinephrine, norepinephrine) in serum. All patients were treated routinely according to EUGOGO recommendations with standard doses of methylprednisolone with standard recommended schedule. Inclusion criterion for the therapy was according to EUGOGO guidelines active, moderate-to-severe and active GO (12 pulses of IVMP 6x0.5g followed by 6x0.25g every week).

NCT ID: NCT04390919 Completed - Clinical trials for Acute Decompensated Heart Failure

Prognostic Factors of Patients With ADHF

Start date: August 2, 2011
Phase:
Study type: Observational

To explore the prognostic indicators for patients with ADHF

NCT ID: NCT04385589 Completed - Heart Failure Clinical Trials

Dapagliflozin in Diabetic Patients (Type 2) With Decompensated Heart Failure

Start date: May 1, 2020
Phase: Phase 4
Study type: Interventional

We hypothesize that Dapagliflozin could improve the diuretic response in diabetic patients with acute decompensated heart failure owing to its diuretic effect in addition to improvement of blood glucose level without remarkable effect on kidney function or electrolytes.

NCT ID: NCT04384653 Completed - Heart Failure Clinical Trials

Crossover Study to Compare the Pharmacokinetics and Bioavailability of a Novel Furosemide Regimen Administered Subcutaneously vs. the Same Dose Administered Intravenously in Subjects With Chronic Heart Failure

Start date: October 17, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

The proposed study aims to compare the pharmacokinetics and bioavailability of intravenous and subcutaneous Furosemide. Although these regimens are not intended to be bioequivalent, they are both expected to achieve therapeutic plasma levels and induce effective diuresis. The test formulation in this study is a buffered solution, Furosemide Injection Solution at 30 mg/mL at pH 7.4 (range 7.0 to 7.8) and is intended for SC injection according to the instructions in the protocol. A commercial formulation of Furosemide Injection, USP will serve as the reference drug in this study, which will be administered by IV bolus. It contains furosemide 10 mg/mL in solution at alkaline pH of 8.0 to 9.3 and is marketed for IV and IM injection. The primary objective of the study is to estimate the absolute bioavailability of furosemide administered by subcutaneous infusion compared with an equivalent dose of furosemide administered by IV bolus administration.

NCT ID: NCT04383080 Completed - Heart Failure Clinical Trials

The Effect and Safety of Low-level Laser Therapy in Acute Decompensated Heart Failure Patients.

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

The advantages of laser acupuncture are a non-invasive, painless, low risk of infection and high safety. Laser acupuncture as a treatment tool has the following advantages1.Painless, 2. Non-invasive treatment, the subject is highly accepted, the risk of infection and needle stick is low, 3. Very few side effects such as fainting, bleeding, 4. The therapeutic dose is easy to operate, and the instrument output frequency, power and time can be controlled. Through the clinical physiological function test plus the verification and analysis of the quantitative test values, it will be more able to define the new role of laser acupuncture treatment in patients with heart failure from the perspective of Chinese medicine.

NCT ID: NCT04379401 Completed - Heart Failure Clinical Trials

Acute Impact of Cardiac Resynchronization on Vascular Function (RVA-CRT)

RVA-CRT
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Evaluation of the effect of short term activation/deactivation of biventricular pacing (BivP) of the CRT (during routine CRT interrogation) on vascular function as assessed via retinal vessel analysis (RVA), in patients treated with CRT.

NCT ID: NCT04375943 Completed - Heart Failure Clinical Trials

Clinical and Echocardiographic Management of Patients With Heart Failure and Diabetes: SCODIAC Follow up Study

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

The study has been carried out to determine diagnostic and therapeutic pathways in a group of HF diabetic patients and to verify whether the use of innovative antidiabetic therapies could modify echocardiographic parameters and influence cardiological therapy.

NCT ID: NCT04371731 Completed - Clinical trials for Heart Failure With Reduced Ejection Fraction

A Single-centre Research Study to Evaluate the Care4Today® Heart Failure Platform.

Start date: May 18, 2015
Phase: N/A
Study type: Interventional

A research study to evaluate the impact of a novel care pathway for patients diagnosed with Heart Failure within Chiltern CCG, supported by an integrated clinical patient record. Assessment of patient outcomes following implementation of Care4Today(R) Heart Failure Platform.

NCT ID: NCT04367051 Completed - Heart Failure Clinical Trials

Pilot Study on Withdrawal of Spironolactone Among Heart Failure With Improved Ejection Fraction

Start date: August 13, 2020
Phase: N/A
Study type: Interventional

The study is a randomized controlled pilot trial to evaluate whether withdrawal of spironolactone is safe and associated with re-deterioration of left ventricular function in patients with heart failure with improved ejection fraction. The aim of current trial is to test the hypothesis that withdrawal of spironolactone would not be associated with relapse of significant clinical deterioration of left ventricular systolic function.