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Heart Failure clinical trials

View clinical trials related to Heart Failure.

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NCT ID: NCT02188784 Completed - Clinical trials for Chronic Heart Failure

Oral Iron Repletion Effects On Oxygen Uptake in Heart Failure

IRONOUT
Start date: August 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if oral iron (FE) polysaccharide is superior to oral placebo in improving functional capacity as measured by change in peak VO2 by CPET (Cardiopulmonary Exercise Testing) , of a broad population of patients with HFrEF (Heart Failure Exercise Testing) and Fe deficiency at 16 weeks. Hypothesis: In a broad population of HFrEF patients with Fe deficiency, compared to oral placebo, therapy with oral Fe polysaccharide will be associated with improvement in functional capacity at 16 weeks as assessed by CPET.

NCT ID: NCT02183792 Completed - Heart Failure Clinical Trials

Aquaresis Utility for Hyponatremic Acute Heart Failure Study

AQUA-AHF
Start date: December 2014
Phase: Phase 4
Study type: Interventional

Hyponatremia is a common finding in acute heart failure (HF) patients and is associated with worse prognosis. In addition to its prognostic value, hyponatremia may have importance during the acute management of HF. We've recently shown that acute or chronic hyponatremia, especially <130 mEq/L, was associated with higher loop diuretic dose requirements and more frequent need for escalation of the diuretic regimen to achieve the same level of diuresis as normonatremic HF patients. Aquaresis with tolvaptan represents a potentially advantageous approach to the management of volume overload in HF, especially in patients presenting with concomitant hyponatremia. The purpose of the current study is to prospectively evaluate the comparative efficacy and safety of a tolvaptan-based diuretic regimen compared to conventional diuresis with a furosemide-based regimen on short-term clinical and treatment outcomes in hyponatremic acute HF patients. This will be a prospective, open-label, parallel-group, randomized study comparing a tolvaptan-based aquaretic regimen to a conventional continuous infusion loop diuretic-based regimen of furosemide. Up to 55 (target sample size of 50) adult subjects admitted with acute HF and signs of volume overload, and serum sodium less than 135 mEq/L will be randomized to tolvaptan or furosemide treatment arms. The initial 24 hours of study treatment will compare tolvaptan monotherapy to furosemide monotherapy. After the initial 24 hours, treatment regimens may be altered to achieve desired clinical goals. Patients will be followed for up to 96 hours and at discharge for study purposes.

NCT ID: NCT02181686 Completed - Heart Failure Clinical Trials

Iperia/Sentus QP Study

Start date: July 2014
Phase: N/A
Study type: Observational

The objective of this study is to confirm the safety and efficacy of the new Sentus OTW QP LV lead and Iperia ICD family. The study focuses on the safety and efficacy of the QP device system.

NCT ID: NCT02180919 Completed - Heart Failure Clinical Trials

Implementation of Telemonitoring in Chronic Heart or Lung Failure

TELECRAFT
Start date: June 2010
Phase: Phase 1
Study type: Interventional

The aims of the study are to: 1. Implement a telemonitoring programme in heart failure and obstructive pulmonary disease (COPD) /chronic respiratory patients by assessing the real world impact of on readmissions, consults, home visits, quality of life and economic endpoints. 2. Explore the effects of telemonitoring across heart and respiratory groups with respect to i) factors that influence how patients integrate telemonitoring into their daily routines and self care behaviour and ii) how healthcare professionals use telemonitoring to aid decision- making. 3. Understand the impact of telemonitoring on a variety of care pathways.

NCT ID: NCT02178579 Completed - Heart Failure Clinical Trials

Prospective Observation of Cardiac Safety With Proteasome Inhibition

PROTECT
Start date: November 2014
Phase:
Study type: Observational

The purpose of this study is to better define and understand potential cardiac toxicities of proteasome inhibitors and to understand optimal management strategies to treat and prevent cardiovascular events.

NCT ID: NCT02177656 Completed - Heart Failure Clinical Trials

Motivational Interviewing Tailored Intervention for Patients With Heart Failure (MITI-HF)

MITI-HF
Start date: January 2012
Phase: N/A
Study type: Interventional

This study will test the effectiveness of motivational interviewing and skill building compared to usual care to improve self-care in heart failure (HF) patients. The target population is HF patients recruited from the Hospital of the University of Pennsylvania after an in-patient admission. Patients in the intervention arms will receive one home-visit from a nurse who does a self-care intervention followed up by 3 follow-up phone calls.

NCT ID: NCT02176174 Completed - Stroke Clinical Trials

Ethnicity and Onset of Cardiovascular Disease: A CALIBER Study

Start date: December 2013
Phase: N/A
Study type: Observational

Specific cardiovascular diseases, such as stroke and heart attack, have been shown to vary by ethnic group. However, less is known about differences between ethnic groups and a wider range of cardiovascular diseases. This study will examine differences between ethnic groups (White, Black, South Asian and Mixed/Other) and first lifetime presentation of twelve different cardiovascular diseases. This information may help to predict the onset of cardiovascular diseases and inform disease prevention strategies. The hypothesis is that different ethnic groups have differing associations with the range of cardiovascular diseases studied.

NCT ID: NCT02173548 Completed - Clinical trials for Heart Failure With Normal Ejection Fraction

Interleukin-1 Blockade in HF With Preserved EF

D-HART2
Start date: September 2014
Phase: Phase 2
Study type: Interventional

- Heart Failure with Preserved Ejection Fraction (HFpEF) is a common form of heart failure - Standard treatment for heart failure, show less than ideal results in HFpEF - Evidence of systemic inflammation is common in all forms of heart failure, including HFpEF - The main hypothesis of this study is that systemic inflammation contributes to heart failure symptoms and exercise limitations in patients with HFpEF - The main objective is to treat patients with HFpEF and evidence of systemic inflammation with an anti-inflammatory drug targeting Interleukin-1 (or placebo) to determine effects on cardiovascular function

NCT ID: NCT02173028 Completed - Clinical trials for Congestive Heart Failure

RESynchronizaTiOn theRapy and bEta-blocker Titration

RESTORE
Start date: June 2013
Phase: N/A
Study type: Observational

Patients will be treated according to the clinical practice of the participating centers and to the international guidelines for the treatment of heart failure.The present analysis provides a collection of data about the changes to drug therapy after the "Cardiac Resynchronization Therapy" (CRT) procedure , and any signs and symptoms of intolerance to prescribed medications.

NCT ID: NCT02170961 Completed - Acute Heart Failure Clinical Trials

Study of Polymorphisms of RAAS and MMPs in Acute Heart Failure

PRA-MMP
Start date: February 2013
Phase:
Study type: Observational

this study aim to investigate the: - association of RAAS polymorphisms and AHF - association of MMP 3 and 12 polymorphisms and AHF