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Ventricular Dysfunction, Left clinical trials

View clinical trials related to Ventricular Dysfunction, Left.

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NCT ID: NCT02763774 Recruiting - Clinical trials for Disorder; Heart, Functional, Postoperative, Cardiac Surgery

Effects a Rehabilitation Program in Patients With Left Ventricular Dysfunction After Coronary Artery Bypass Grafting

Start date: June 2014
Phase: N/A
Study type: Interventional

This study aims to analyze effects of three types of cardiac rehabilitation protocol on fuctional capacity, inflammatory markers, pulmonary function and clinical outcomes after coronary artery bypass grafting (CABG) in patients with left ventricular disfunction. Patients will be randomized and allocated in three groups according to type of exercise protocol: 1. walk; 2. cycle; 3. functional electrical stimulation.

NCT ID: NCT02557217 Recruiting - Clinical trials for ST Elevation Myocardial Infarction

NP202 for Treatment of Post -STEMI Left Ventricular Systolic Dysfunction

Start date: October 2015
Phase: Phase 2
Study type: Interventional

NP202 is an experimental drug being developed by Armaron Bio Pty Ltd for potential use as a treatment for people after they have had a heart attack (MI).

NCT ID: NCT02449330 Recruiting - Clinical trials for Diabetes Mellitus, Type 2

Teneligliptin on the Progressive Left Ventricular Diastolic Dysfunction With Type 2 Diabetes Mellitus Study

TOPLEVEL
Start date: June 2015
Phase: Phase 4
Study type: Interventional

This is the clinical trial designed to assess the cardiac diastolic function of long term treatment with teneligliptin compared to that without teneligliptin in patients with type 2 diabetes mellitus by two arms; one includes patients showing E/e' by echocardiography less than 8, the other includes patients showing E/e' by echocardiography more than 8.

NCT ID: NCT01870310 Recruiting - Heart Failure Clinical Trials

Renal Denervation in Patients With Heart Failure and Severe Left Ventricular Dysfunction.

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

It is a randomized prospective controlled study evaluating the effect of transcatheter renal denervation on the clinical status of patients with chronic heart failure and its safety procedures. The working hypothesis of the study is that by performing transcatheter renal denervation in patients with chronic heart failure and severe left ventricular systolic dysfunction there will a resultant reduction in the renal sympathetic activation which in turn will reduce the number of hospitalizations and deaths from heart failure.

NCT ID: NCT01747187 Recruiting - Septic Shock Clinical Trials

Cardiac Stress in Septic Shock - Biomarkers, Echocardiography and Outcome

Septic Heart
Start date: October 2012
Phase: N/A
Study type: Observational

Septic shock is a major cause of death in intensive care. Septic shock is often dominated by profound changes in organ functions, of which cardiac failure is one of the most severe. In septic shock, biological markers of cardiac stress are often elevated. It is not known to what extent this indicates structural damage to the heart, or in what way they correlate to echocardiographic signs of heart failure. Here, cardiac failure in ICU patients with septic shock is studied, using biological markers of cardiac stress, inflammatory parameters and echocardiography. Investigators hypothesize that biomarkers of cardiac stress correlate with echocardiographic signs of heart failure, and that they can predict an increased risk of death.

NCT ID: NCT01267331 Recruiting - Clinical trials for Left Ventricular Dysfunction

Cell Therapy in Patients With Chronic Ischemic Heart Disease Undergoing Cardiac Surgery

Start date: December 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This prospective, randomized, placebo-controlled study was designed to assess the safety, feasibility and efficacy of intramyocardial injection of autologous bone marrow mononuclear cells in patients with severe, chronic ischemic disease scheduled to coronary artery bypass surgery.

NCT ID: NCT00512005 Recruiting - Heart Failure Clinical Trials

VIVID - Valvular and Ventricular Improvement Via iCoapsys Delivery - Feasibility Study

VIVID
Start date: January 2008
Phase: Phase 1
Study type: Interventional

The purpose of this prospective, non-randomized, single-arm feasibility study is to evaluate safety and feasibility of the iCoapsys System in patients with functional mitral valve insufficiency caused by annular dilation and/or papillary muscle displacement.

NCT ID: NCT00188994 Recruiting - Clinical trials for Left Ventricular Dysfunction

Insulin Cardioplegia for Poor Left Ventricular Function

Start date: August 1999
Phase: N/A
Study type: Interventional

The purpose of this investigation is to develop a means to improve the recovery of cardiac metabolism and ventricular function following coronary artery bypass surgery (CABG) in patients with poor preoperative ventricular function (e.g. ejection fraction <40%).