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Heart Transplantation clinical trials

View clinical trials related to Heart Transplantation.

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NCT ID: NCT00574197 Completed - Clinical trials for Heart Transplantation

Enteric-coated Mycophenolate Sodium (Myfortic®) in Heart Transplant Recipients

Start date: June 2006
Phase: Phase 4
Study type: Interventional

Mycophenolate sodium (Myfortic®) is a newly developed enteric-coated tablet version of mycophenolate mofetil (Cellcept®) which is currently used as therapy for the prevention of transplant rejection. Myfortic® was developed to improve the gastrointestinal tolerability of Cellcept®. The new enteric-coated, Myfortic® is presently FDA approved for the prevention of acute kidney rejection only. There is no clinical data of its use in heart transplant patients.

NCT ID: NCT00531921 Completed - Clinical trials for Kidney Transplantation

Effects of Donor and Recipient Genetic Expression on Heart, Lung, Liver, or Kidney Transplant Survival

Start date: September 2007
Phase: N/A
Study type: Observational

Activity of genes in donor tissues that are involved in inflammation are thought to be involved with early organ dysfunction, increased immune responses in transplant recipients, and organ rejection. The purpose of this study is to determine the relationship between genetic expression in donor and recipient tissue with transplant survival. Participants in this study will have received heart, lung, liver, or kidney transplants.

NCT ID: NCT00521573 Completed - Clinical trials for Heart Transplantation

Effects of Chocolate on Coronary Vasomotion in Patients After Heart Transplantation

Start date: n/a
Phase: Phase 1
Study type: Interventional

The aim of the present study is to investigate whether the ingestion of a flavonoid-rich dark chocolate compared to flavonoid-free placebo chocolate will improve coronary vasomotion in heart transplanted patients.

NCT ID: NCT00497757 Completed - Clinical trials for Heart Transplantation

Induction of Donor Specific Tolerance in Recipients of Cardiac Allografts by Donor Stem Cell Infusion

Start date: July 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of this research study is to establish chimerism and avoid graft-versus-host disease in patients who need a heart transplant.

NCT ID: NCT00469911 Completed - Clinical trials for Heart Transplantation

Quantification of Intramyocardial Lipid by Proton Magnetic Resonance Spectroscopy

MRS
Start date: August 2005
Phase: N/A
Study type: Interventional

Accumulation of triglycerides in heart tissue has been associated with changes in left ventricular function which can lead to heart failure. Proton magnetic resonance spectroscopy is currently the only non-invasive in vivo method to measure myocardial triglycerides content. The primary goal of this study was to determine if Magnetic Resonance Spectroscopy could effectively measure myocardial triglyceride content in myocardial heart tissue. Thus, quantitative and reliable techniques to monitor in vivo triglyceride accumulation in the heart are important for disease diagnosis and management. Currently, no such imaging method exists.

NCT ID: NCT00449059 Completed - Hypertension Clinical Trials

Nitrate and Hypertension in Heart Transplanted Patients

Start date: January 2003
Phase: Phase 4
Study type: Interventional

The aim of the study was to evaluate the acute effect of nitroglycerine infusion on blood pressure and heart rate in heart-transplanted patients with cyclosporine-induced hypertension.

NCT ID: NCT00359814 Completed - Clinical trials for Heart Transplantation

Exchange of Azathioprine by Mycophenolatmofetile and Cyclosporine A Dose Reduction After Heart Transplantation

Start date: November 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to improve or save renal function by optimizing the immunosuppressive regimen by reducing the Cyclosporine A dose and the exchange of Azathioprine by Mycophenolatmofetile, which is an effective immunosuppressive agent and will minimize the risk of acute rejection episodes.

NCT ID: NCT00359658 Completed - Clinical trials for Heart Transplantation

Withdrawal of Steroids, Cyclosporine A Dose Reduction and Switch to Mycophenolatmofetile After Heart Transplantation

Start date: November 2004
Phase: N/A
Study type: Interventional

The purpose of this study is first to improve or save renal function and second to decrease cardiac risk factors by optimising the immunosuppressive regimen by withdrawing steroids and reducing the Cyclosporine A dose. The concomitant administration of Mycophenolatmofetile, an effective immunosuppressive agent, will minimize the risk of acute rejection episodes.

NCT ID: NCT00297830 Completed - Clinical trials for Liver Transplantation

Zoledronic Acid Versus Alendronate for Prevention of Bone Loss After Organ Transplantation

CTX
Start date: November 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness and safety of zoledronic acid with alendronate in the prevention of bone loss after organ transplantation. Zoledronic acid is given as a single intravenous infusion. Alendronate is given as a weekly pill. Both are expected to be very effective, but it is not known which one will work best.

NCT ID: NCT00264355 Completed - Acute Renal Failure Clinical Trials

Metabolic Pattern of Cyclosporine A and Acute Renal Failure

Start date: December 2005
Phase: Phase 4
Study type: Interventional

Following heart transplantation many patients develop acute renal failure in the early posttransplant phase and some are in need of renal replacement therapy for shorter or longer time. The cause of this acute renal failure is most probably multi factorial but many reports indicate that cyclosporine has a central role in the pathophysiology and it is generally recommended to lower the cyclosporine load to patients developing acute renal failure in this population. Several in vitro studies on renal cells in culture indicate that the primary metabolites of cyclosporine (AM1, AM9, AM4N) are less toxic to the kidney than cyclosporine itself. However, the secondary metabolite AM19 as well as the cyclic metabolites AM1c and AM1c9 has been associated with decreased renal function and nephrotoxicity renal transplant recipients. The primary objective of this pilot study is to investigate if the concentrations of secondary- and cyclic metabolites of cyclosporine (AM19, AM1c, AM1c9) is related to development of acute renal failure in the early posttransplant phase following heart transplantation. Secondary objectives are to investigate associations between genotypes of P-glycoprotein and CYP3A5 and the metabolic pattern of cyclosporine.