Clinical Trials Logo

Kidney Failure, Chronic clinical trials

View clinical trials related to Kidney Failure, Chronic.

Filter by:

NCT ID: NCT01564966 Completed - Hypertension Clinical Trials

Cardiovascular-Renal Consequences of Reducing Renal Mass After Living Kidney Donation

Start date: April 2008
Phase: N/A
Study type: Observational

- A reduce in renal mass may result in remnant single nephron hyperfiltration, with associated proteinuria and an accelerated loss of kidney function. - Live-donor kidney transplantation is generally considered the best choice for patients who have renal failure and are awaiting transplantation, because these kidneys function better than kidneys from deceased donors, and waiting times for deceased-donor transplants are long - Although several studies have shown that kidney donation has low short-term morbidity and mortality, the data on long-term outcomes are much less complete. - This study is designed to prospectively evaluate the effects of unilateral nephrectomy on cardiovascular-renal functions of donors after living kidney donation: the development of hypertension, albuminuria, renal failure, inflammatory and endothelial changes.

NCT ID: NCT01554982 Completed - Clinical trials for End Stage Renal Disease

A Long-Term Safety Extension Trial of Ferric Citrate in Patients With End-Stage Renal Disease (ESRD) on Dialysis

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

A long-term safety study of ferric citrate (KRX-0502) in renal failure patients who have completed study KRX-0502-304. Only patients who participated in the KRX-0502-304 trial may participate in this trial.

NCT ID: NCT01536548 Completed - Clinical trials for Chronic Kidney Disease

Indicating Direction and Angle for Cannulating of AV-fistula in Hemodialysis Patients

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

Arteriovenous fistula is the preferred access for hemodialysis, and cannulation using a "button-hole" technique is increasingly recommended. By using the same two sites for cannulation there are reports of less risk of complications and less pain for the patient. However, button-hole cannulation can be difficult for the dialysis nurse, and failing cannulations can damage the AV fistula and increase patient discomfort. The investigators therefore will test whether a simple marking on the skin of the direction and angle of cannulation used in each specific patient could improve the probability of a successful and painfree cannulation.

NCT ID: NCT01471041 Completed - Clinical trials for End Stage Renal Disease

Safety and Efficacy Study of the Venous Window Needle Guide to Access Arteriovenous (AV)Fistulae

SAVE
Start date: December 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The SAVE Study will evaluate the safety and efficacy of the Venous Window Needle Guide in achieving access of a deep, un-cannulatable arteriovenous fistula to complete hemodialysis as prescribed.

NCT ID: NCT01447368 Completed - Vascular Diseases Clinical Trials

Cinacalcet Versus Parathyroidectomy in Peritoneal Dialysis Patients

PROCEED
Start date: May 10, 2010
Phase: Phase 4
Study type: Interventional

This is a pilot, prospective randomized controlled study with the primary objective to evaluate and compare medical treatment of severe SHPT, namely oral cinacalcet versus surgical treatment, that is, parathyroidectomy with forearm autografting, on the progression of coronary artery and valvular calcification and left ventricular mass index in endstage renal disease patients receiving peritoneal dialysis over 12 months. The change in arterial stiffening, left ventricular volume, aortic valve calcium score and bone mineral density, nutritional status and biochemical parameters, quality of life measures will be evaluated as secondary objectives of this study.

NCT ID: NCT01446302 Completed - Clinical trials for Kidney Failure, Chronic

Metabolic and Inflammatory Responses to Hemodialysis and the Effect of a Meal

Start date: October 2011
Phase: N/A
Study type: Interventional

The objective of this study is to characterize the hormonal and inflammatory responses to hemodialysis, and to determine the effect of a meal versus fast on the metabolic changes in the post-dialytic phase.

NCT ID: NCT01429038 Completed - Kidney Failure Clinical Trials

Mesenchymal Stem Cells After Renal or Liver Transplantation

Start date: February 1, 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The immune system of a patient can attack the liver or the kidney received from a donor (organ rejection). This can be prevented by treating these patients long-life with immunosuppressive drugs. Unfortunately, these drugs lead to numerous side effects and fail to prevent the rejection occurring months later after the transplantation (chronic rejection). Recently, it has been shown that a particular type of cells present in the bone marrow, namely Mesenchymal Stem Cells (MSC), when injected to a patient, suppress its immune system and increase success rates of blood cells transplantation. This outcome opens doors to investigate the potential of these cells to provide a valuable tool for improving solid organ transplantation without the need of high concentration of immunosuppressive drugs. The present project aims at evaluating the safety and tolerability of MSC administration after liver or kidney transplantation.

NCT ID: NCT01423955 Completed - Renal Failure Clinical Trials

Erythropoietin (EPO) to Protect Renal Function After Cardiac Surgery

EPRICS
Start date: October 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the potential of erythropoietin in reducing risk and degree of acute kidney injury after cardiac surgery.

NCT ID: NCT01380847 Completed - Clinical trials for Kidney Transplantation

Prediction of Chronic Allograft Nephropathy

Prefigur
Start date: June 2011
Phase:
Study type: Observational

The investigators have shown that epithelial-to-mesenchymal transition (EMT) markers in early protocol biopsies of the renal allograft predicts the progression of fibrosis during the first year post-transplantation. The investigators will develop a non-invasive approach for predicting fibrosis as a substitute for the invasive allograft biopsy procedure, by longitudinal assessment of the mRNA expression level of genes implicated in EMT/fibrogenesis and inflammation in urinary cells from kidney transplant recipients during the first year post-transplantation.

NCT ID: NCT01356966 Completed - Clinical trials for Kidney Failure, Chronic

Exercise Intolerance in Renal Failure

EIRF
Start date: May 2011
Phase: Phase 2
Study type: Interventional

Patients with chronic kidney disease have profound exercise intolerance which contributes to an increased risk of cardiovascular disease. The investigators have found that chronic kidney disease patients have an exaggerated increase in blood pressure during certain forms of exercise that could certainly contribute to exercise dysfunction as well as cardiovascular risk. The investigators will test the mechanisms underlying this exaggerated blood pressure response, as well as the potential benefits of short-term tetrahydrobiopterin (BH4) with folic acid on both exercise dysfunction and cardiovascular risk factors in chronic kidney disease. The investigators will test whether short-term treatment with tetrahydrobiopterin (BH4), a cofactor for nitric oxide, together with folic acid improves inflammation, vascular health, and adrenaline levels, both at rest and during exercise in chronic kidney disease.