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Heart Failure clinical trials

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NCT ID: NCT01614652 Terminated - Clinical trials for Congestive Heart Failure

A Pivotal Trial to Establish the Efficacy and Long-term Safety of the Parachute Implant System

PARACHUTE IV
Start date: December 2012
Phase: Phase 3
Study type: Interventional

Treatment of ischemic heart failure.

NCT ID: NCT01605019 Terminated - Heart Failure Clinical Trials

The Use of CoSeal (Sealant Agent) in Patients During Left Ventricular Assist Device Surgery

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the use of a device called CoSeal™. CoSeal™ is an FDA approved synthetic (man-made) surgical sealant which is currently used to help stop leaks in blood vessels during surgery. This study is evaluating CoSeal™ when it is applied to various areas of the heart during the surgery to implant a Left Ventricular Assist Device (LVAD). the investigators are looking for evidence which indicates that CoSeal™ may be useful in reducing or stopping bleeding, the occurrence of micro emboli (small particles of air or blood), and the formation of cardiac adhesions (scar tissue strands that may form around the heart in the area of a previous LVAD operation) in patients who undergo LVAD implantation surgery.

NCT ID: NCT01583881 Terminated - Hypertension Clinical Trials

Denervation of the renAl sympathetIc nerveS in hearT Failure With nOrmal Lv Ejection Fraction

DIASTOLE
Start date: April 1, 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Increasing evidence suggests an important role of activation of the sympathetic nervous system (SNS) in the clinical phenomena of heart failure with normal left ventricular ejection fraction and hypertension. The current study aims to evaluate efficacy and safety of renal sympathetic denervation for the modulation of the SNS in patients with heart failure with normal LV ejection fraction.

NCT ID: NCT01558674 Terminated - Heart Failure Clinical Trials

A Study of MK-7145 in Participants With Renal Insufficiency (Part I) and Heart Failure With Renal Insufficiency (Part II) (MK-7145-011)

Start date: May 23, 2014
Phase: Phase 1
Study type: Interventional

Part I is a 3-period, active comparator-controlled, fixed sequence study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of MK-7145 compared to furosemide in participants with moderate-to-severe renal insufficiency (RI) without heart failure (HF). Primary hypothesis for Part I is that at least one well-tolerated dose of MK-7145 will produce a greater 24hr urinary excretion of sodium (UNa) on the 1st day of MK-7145 dosing than 80 mg furosemide (on the 1st day of furosemide dosing) in participants with moderate-to-severe RI. If MK-7145 is safe at natriuretic doses in RI in Part I of this study, MK-7145 will be investigated in participants with heart failure (HF) and RI (Part II). Part II is 4 period, fixed sequence, active comparator controlled (in Period 1), titration (in Periods 2, 3 and 4) study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of a titration regimen of MK-7145 compared to an optimized stable maintenance regimen of furosemide or torsemide in participants with New York Heart Association (NYHA) Class II and III heart failure and moderate or severe renal insufficiency. The primary hypothesis for Part II is that at least one dose of MK-7145, titrated according to a fixed dose titration regimen, will be associated with a reduction in N-terminal pro-brain natriuretic peptide (NT-proBNP) compared to furosemide or torsemide (at 24 hours post morning dose on the last dosing day of each period) in participants with NYHA class II/III HF with moderate or severe RI.

NCT ID: NCT01549158 Terminated - Clinical trials for Compensated Heart Failure

Single Dose Study to Compare the Pharmacodynamics of Torasemide-PR 10 mg,Torasemide-IR 10 mg and Furosemide-IR 40 mg in Patients With Compensated Heart Failure

Start date: February 2012
Phase: Phase 4
Study type: Interventional

This is a randomized, open-label, blinded-endpoint, crossover, single dose study to compare the pharmacodynamics of Torasemide-PR 10 mg, Torasemide-IR10 mg and furosemide-IR 40 mg. 30 patients of both sexes with CHF with a maximum imbalance of 60:40% in either direction will be included in the study. Patients with compensated heart failure, grade II or III as defined by the European Society of Cardiology, with a duration of ≥ 3 months at the time of inclusion documented in the patient's record or patients who previously required diuretic therapy. Principal variable will be the efficiency of sodium excretion that will be assessed as the ratio between the average drug-induced natriuresis and the average drug recovered in urine over 24 hours. The difference between the efficiency of 24 hour sodium excretion following administration of torasemide PR and furosemide will be formally tested by means of a Students t-test for paired samples. The test will be two-sided at 5% significance level. Efficiency changes over time will also be assessed, however will not be subject to formal statistical testing.

NCT ID: NCT01541202 Terminated - Clinical trials for Chronic Heart Failure

Study of the Survival of Recombinant Human Neuregulin-1β in Chronic Heart Failure (CHF) Patients

Start date: February 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate efficacy of rhNRG-1 in reducing the death rate of heart failure.

NCT ID: NCT01535196 Terminated - Clinical trials for Chronic Heart Failure

Vitamine D Treatment in Chronic Heart Failure

Start date: December 2012
Phase: Phase 3
Study type: Interventional

The investigators hypothesized that in vitamin D deficiency the 25-OH-D3 vitamin substitution improve the heart function in chronic heart failure. Type of study: Controlled, randomized, double blind, placebo control Number of patient: 300; 150 treated and 150 placebo controlled Type of drug: 180 000 IU 25-OH-D3 vitamin oil (Vigantol) per month in the 0,1,2,3,6, month Duration of study:1+1 year Primary end points: Survival rate, Ejection fraction by ultrasound, Brain natriuretic peptid, Secondary end points: Safety of D-vitamin supplementation, well being score, blood pressure, BMI Walking distant in 6 minutes Visits: Screening, Randomization, 1month, 2 month, 3 month, 6 month, 12 month, 24 month,

NCT ID: NCT01522378 Terminated - Clinical trials for Congestive Heart Failure

Cardiac Resynchronization and Iodine Meta-Iodobenzylguanidine (MIBG) Imaging

Start date: February 2012
Phase: Phase 1
Study type: Interventional

Subjects were recruited if their healthcare provider decided that they needed treatment with a special Internal Cardiac Defibrillator (ICD) called a biventricular ICD. The investigators did this study to see if part of the nerve organ, called the sympathetic nervous system, may be responsible for the improvement seen in patients that receive biventricular pacing. The investigators had three ways to measure sympathetic nervous activity: 1) by using a special blood sample, 2) by monitoring heart rhythm, and 3) by performing a special heart scan.

NCT ID: NCT01520714 Terminated - Clinical trials for Congestive Heart Failure

Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds (EXPECT)

EXPECT
Start date: December 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether changes in a patient's position affect LV capture thresholds in a clinically significant way.

NCT ID: NCT01512381 Terminated - Heart Failure Clinical Trials

Atrioventricular Node Ablation in Patients With Atrial Fibrillation and Moderate Chronic Heart Failure

VISTA
Start date: December 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether cardiac resynchronization therapy (CRT) is superior to interventricular right ventricle (RV) septal pacing in respect of reverse remodeling (LV ESD) and morbidity in patients with less preserved (less than 45%) ejection fraction (EF), persistent/permanent atrial fibrillation (AF) who successfully received atrioventricular (AV) junction ablation ablation (100% pacemaker dependency)