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Kidney Failure, Chronic clinical trials

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NCT ID: NCT01595984 Active, not recruiting - Kidney Failure Clinical Trials

Comparison of Efficacy and Safety of Treatment With a Calcineurin Inhibitor (CNI)Versus a CNI-free Treatment in Renal Transplantation (CIME)

CIME
Start date: May 3, 2012
Phase: Phase 3
Study type: Interventional

The main objective of this protocol is to compare the impact on renal function of two different immunosuppressive regimens in patients with de novo renal transplant. Renal function will be accurately evaluated by measuring the clearance of iohexol. The protocol will also evaluate the efficacy and safety in a short term of these two different immunosuppressive regimens.

NCT ID: NCT01580046 Recruiting - Clinical trials for Kidney Failure, Chronic

Renal Toxicity of Iodixanol and Iopromide in Patients With Renal Dysfunction

RIPE
Start date: April 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare renal toxicity of Iodixanol and Iopromide in patients with renal dysfunction.

NCT ID: NCT01569698 Terminated - Clinical trials for Kidney Failure, Acute

Modalities of Renal Replacement Therapy in Pediatric Acute Kidney Injury

EPURE
Start date: June 2012
Phase:
Study type: Observational

Limited prospective data is available to compare morbidity and mortality between renal replacement modalities in pediatric acute renal failure. In the absence of clear standard of care, the choice of the extra renal replacement therapy modality is subject to clinical judgement, practical aspects, and costs. This study will supply important data about usual modalities of pediatric acute extra renal replacement therapy and their impact on patient outcome and renal recovery. An obvious next step will be to conduct a randomized controlled trial comparing the different strategies.

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: NCT01537315 Terminated - Clinical trials for Cardiovascular Disease

Hydroxychloroquine in Cardiovascular Disease in Patients With Chronic Kidney Disease: A Proof of Concept Study

Start date: February 2012
Phase: Phase 2
Study type: Interventional

Presence of multiple traditional and nontraditional risk factors of atherosclerosis and cardiovascular disease (CVD) including inflammation in patients with chronic kidney disease (CKD) contribute to high CVD morbidity and mortality in this patient population. Additionally, the traditional approaches towards the therapy of CVD have little impact on CV mortality in these patients. Hydroxychloroquine (HCQ) used as anti-inflammatory in rheumatological disorders, has multiple beneficial properties relevant to the process of vascular disease. The effects of HCQ on atherosclerosis (AS) and vascular disease in CKD is not known yet. Thus, the study hypothesis is that HCQ treatment in individuals with CKD will provide clinically significant benefit in the management of CVD and will provide biological and functional atherosclerotic benefits.

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: NCT01515878 Recruiting - Clinical trials for Cardiovascular Diseases

Hemocontrol's Effectiveness on the Reduction of Cardiovascular Long-term EventS

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

It is hypothesized that a consistent use of the Hemocontrol TM biofeedback function improves long-term cardiovascular outcome, mediated by reduced hypertension due to fluid overload and by reduced incidence of intradialytic hypotensive episodes

NCT ID: NCT01510795 Enrolling by invitation - Clinical trials for Kidney Failure, Chronic

Mineralocorticoid Receptor Antagonist and Kidney Allograft Histology

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

Chronic allograft nephropathy is one of dominant causes of long term kidney transplant failure. Its main histological determinant is interstitial fibrosis and tubular atrophy. Mechanisms of these changes are multifactorial and are not completely elucidated. Epithelial mesenchymal transition (EMT) might be one of the mechanisms. On molecular level role of renin angiotensin aldosterone system (RAAS) has been recognized. Recently, mineralocorticoid hormone aldosterone has been proposed as a possible direct contributor to the progression of renal injury and fibrosis, beside his well known role as a regulator of extracellular fluid volume and sodium and potassium balance. In this study the investigators will determine the impact of mineralocorticoid receptor antagonist use on progression of chronic scores in transplanted kidney over one year. The investigators hypothesis is that spironolactone use in kidney transplant patients will slow down progression of chronic histological changes- interstitial fibrosis, tubular atrophy and arteriolar hyalinosis.

NCT ID: NCT01481610 Terminated - Clinical trials for Kidney Failure, Chronic

Safety Study of Renal Function in Patients With Chronic Kidney Failure Taking Lumiracoxib or Diclofenac for Arthralgia

Start date: January 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the use of lumiracoxib in this particular population is associated with a decrease in glomerular filtration rate (GFR) compared to diclofenac; and to compare the magnitude of such impairment, if any, associated with use of lumiracoxib and diclofenac.