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Cardiac Failure clinical trials

View clinical trials related to Cardiac Failure.

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NCT ID: NCT03332186 Completed - Clinical trials for Congestive Heart Failure

A Study of Experimental Medication BMS-986231 in Patients With Different Levels of Kidney Function

Start date: March 15, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate experimental medication BMS-986231 in patients with different levels of kidney function.

NCT ID: NCT03243604 Completed - Clinical trials for Arrhythmias, Cardiac

cARdiotoxicity Profile of aBIraTeRone in prostAte Cancer : a pharmacoviGilancE Study

ARBITRAGE
Start date: May 16, 2017
Phase:
Study type: Observational

Abiraterone associated with prednisone is used in prostate cancer. Abiraterone is a selective small-molecule inhibiting cytochrome P450 17A1 (CYP17A1), a key enzyme in androgen synthesis. CYP17A inhibition is also responsible for mineral corticosteroid related adverse events as hypokaliemia, fluid retention, and hypertension. Primary hyperaldosteronism is associated with cardiovascular toxicities such as atrial fibrillation and cardiac failure. Other androgen-deprivation therapies are not associated with increased mineral corticosteroid level. This study investigates reports of cardiovascular toxicities for treatment including L02 (sex hormones used in treatment of neoplastic diseases), and G03 (sex hormones) used in prostate cancer in the French pharmacovigilance database and in the EudraCT database.

NCT ID: NCT03212898 Completed - Atrial Fibrillation Clinical Trials

Pharmacist Interventions in Rural Elderly Warfarin Patients

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

The primary study goal is to explore the influence of pharmacist interventions on the effectiveness of warfarin treatment in a specific subpopulation.

NCT ID: NCT03197792 Recruiting - Clinical trials for Pulmonary Hypertension

Perioperative Portal Vein Pulsatility as a Postoperative Prognostic Indicator in Pulmonary Endarterectomy

PVP-ETO-CPC
Start date: May 26, 2017
Phase: N/A
Study type: Interventional

The investigators aim to evaluate the utility of portal vein pulsatility as a predictor of the composite outcome of persistent organ dysfunction plus death in patients undergoing elective or urgent pulmonary endarterectomy for thromboembolic pulmonary hypertension. The investigators' hypothesis is that the portal vein pulsatility fraction, measured using transesophageal echocardiography immediately after weaning of cardiopulmonary bypass, is proportional to the risk of developing subsequent end-organ dysfunction in the postoperative setting.

NCT ID: NCT03096678 Recruiting - Cardiac Failure Clinical Trials

Prognosis of Patients With Compete Left Bundle Branch Block

Start date: January 1, 2010
Phase: N/A
Study type: Observational [Patient Registry]

The investigators sought to evaluate the morphological and functional changes, risk stratification and prognosis of patients of participants with compete left bundle branch block (CLBBB). The conduction of this study was largely due to the increased clinical requirement, which reflected the increased awareness among physicians of heart failure due to asynchronous cardiac function caused by CLBBB. The investigators also aim to figure out the time point or CMR parameters for cardiac resynchronization therapy in patients with CLBBB.

NCT ID: NCT03037710 Completed - Cardiac Failure Clinical Trials

Link-HF: Multisensor Non-invasive Telemonitoring System for Prediction of Heart Failure Exacerbation

LINK-HF
Start date: June 2015
Phase:
Study type: Observational

This is a multi-center, non-randomized, non-interventional study to evaluate the accuracy of a remote monitoring and analytical platform for prediction of heart failure exacerbation. The platform acquires continuous multivariate vital signs from HF patients using a new ambulatory wearable (attached by an adhesive) multi-sensor device and analyzes the data using a novel machine learning algorithm.

NCT ID: NCT02939157 Completed - Clinical trials for Heart Failure, Congestive

Pocket-sized Ultrasound for Point-of-care Diagnosis of Heart Failure

POCUS
Start date: December 12, 2016
Phase:
Study type: Observational

Assessment of pocket sized ultrasound (Vscan GE Healthcare) for diagnosing heart failure in primary care patients, with a comprehensive cardiac ultrasound examination (Siemens Acusan P10) performed at a specialized the eco.lab, as reference.

NCT ID: NCT02932566 Completed - Cardiac Failure Clinical Trials

The Efficacy and Safety of Pirfenidone in Patients With Heart Failure and Preserved Left Ventricular Ejection Fraction

PIROUETTE
Start date: March 2, 2017
Phase: Phase 2
Study type: Interventional

This randomised, double-blind, placebo-controlled, phase 2 study aims to evaluate the efficacy and safety of the anti-fibrotic drug pirfenidone in the treatment of patients with heart failure and preserved left ventricular ejection fraction (HFpEF). Participants will be randomised to receive either pirfenidone or placebo, for a period of 12 months.

NCT ID: NCT02859636 Terminated - Cardiac Failure Clinical Trials

Pronostic Value of Endothelial Dysfunction in Heart Failure

Pro-ICARD
Start date: October 2012
Phase: N/A
Study type: Observational

The main objective is to evaluate the pronostic value of endothelial dysfonction in acute heart failure on a combined criteria associating cardiovascular mortality, nex hospitalisation for decompensated heart failure, cardiac graft or ventricular assistance 2 month and 1 year before acute heart failure.

NCT ID: NCT02669134 Withdrawn - Cardiac Failure Clinical Trials

CRT Improved Clinical Response UK Trial

CRICKET
Start date: March 2016
Phase: Phase 3
Study type: Interventional

The main objective of the CRICKET study is demonstrate that AV and VV optimization using SonR improves LV reverse remodeling response to CRT, compared with 'Fixed Settings' (FS) after 6 months of treatment. In this investigator-initiated, multi-centre, 2:2 factorial design, randomized, two-arm, double-blinded, cross-over, prospective trial, CRT recipients will be randomized to 'SonR' atrioventricular (AV) and ventricular-ventricular (VV) optimization or 'fixed settings'. The primary endpoint is an absolute reduction in left ventricular end-systolic volume.