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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT00369382 Completed - Kidney Failure Clinical Trials

Study Of The Safety And Efficacy Of Conversion From A CNI To Sirolimus In Renally-Impaired Heart Transplant Recipients

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

The primary purpose of this study is to determine whether converting from calcineurin inhibitor (CNI) therapy to sirolimus therapy will be more effective than continuing calcineurin inhibitor therapy with respect to renal function in cardiac transplant recipients with mild to moderate renal dysfunction.

NCT ID: NCT00368901 Completed - Clinical trials for Chronic Kidney Disease

STAAR-2 Clinical Study

Start date: January 2002
Phase: Phase 4
Study type: Interventional

To assess the effect of Aranesp on the hemoglobin (Hgb) of CRI subjects who are recombinant human erythropoietin (rHuEPO)-naïve or converting from rHuEPO therapy.

NCT ID: NCT00368368 Completed - Clinical trials for Diabetes Mellitus Type 2

A Study of the Effect of Renal Impairment on the Activity of GK Activator (2) in Patients With Type 2 Diabetes.

Start date: January 2006
Phase: Phase 1
Study type: Interventional

This study will investigate the effect of renal impairment on the pharmacokinetics/pharmacodynamics of GK Activator (2) in patients with type 2 diabetes, and will evaluate the effect of renal function on the safety of the drug. Patients will be assigned to treatment groups according to their renal function (normal, moderate renal impairment, or severe renal impairment). After a 1 week washout period from current oral anti-diabetic treatment, all patients will receive a single oral dose of 100mg GK Activator (2), and blood and urine samples will be taken up to 96h post-dose. The anticipated time on study treatment is <3 months, and the target sample size is <100 individuals.

NCT ID: NCT00365911 Completed - Healthy Clinical Trials

Prevalence of Renal Failure and Risk Factors in an Unreferred Healthy Population

Start date: March 2006
Phase: N/A
Study type: Interventional

Blood sample is taken for measurement of serum creatinine, cystatin C, clone V haemoglobin, cholesterol, urine acid, glycemia and CRP. The medical file is gathered. There will be searched for an association between renal function and cardiovascular risk factors and risk factors by exposition to toxic substantia during work.

NCT ID: NCT00364494 Terminated - Kidney Failure Clinical Trials

Hemodilution and Outcome in Cardiac Surgery

Start date: November 2006
Phase: N/A
Study type: Interventional

An hematocrit of 21-25% is supposed to perform the best organ protection during cardiopulmonary bypass for cardiac surgery. The investigators want to establish the best timing for a transfusion (in patients with a predicted low hematocrit during cardiopulmonary bypass) and the efficacy of preprocedural hemodilution (in patients with a predicted high hematocrit during cardiopulmonary bypass) in patients undergoing cardiac surgery.

NCT ID: NCT00364260 Completed - Anemia Clinical Trials

A Safety and Efficacy Study for Epoetin Alfa in Pre-dialysis Subjects.

Start date: December 1997
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if using Eprex, to maintain hemoglobin within the normal range, will prevent or delay the progression of left ventricular mass growth.

NCT ID: NCT00358813 Completed - Vomiting Clinical Trials

Observational Pharmacokinetic Study Of GW679769 In Subjects With Renal Impairment

Start date: September 8, 2006
Phase: Phase 1
Study type: Interventional

The purpose of the study is to evaluate how subjects with mild or moderate kidney problems process or breakdown the study drug GW679769 in their bodies as compared to healthy subjects.

NCT ID: NCT00358722 Terminated - Clinical trials for Chronic Kidney Failure

An Evaluation of the Long-term Safety of Magnesium Iron Hydroxycarbonate

ALCON
Start date: July 2006
Phase: Phase 2
Study type: Interventional

Fermagate is a phosphate binder that absorbs phosphate from food, reducing the amount that the body can absorb. The purpose of this study it to look at the safety of fermagate over longer periods of time.

NCT ID: NCT00358306 Completed - Clinical trials for Endothelial Dysfunction

The Role of Endothelium Dysfunction in Progression of CKD (Chronic Kidney Disease) After AKI (Acute Kidney Injury)

Start date: April 2008
Phase:
Study type: Observational

To understand how AKI (Acute Kidney Injury) leads to chronic kidney disease so therapies can be found to alter the progression of events thereby significantly impacting the long-term outcomes of children who develop AKI.

NCT ID: NCT00358046 Active, not recruiting - Kidney Diseases Clinical Trials

Efficacy and Tolerability of ILY101 in Dialysis Patients With Hyperphosphatemia

Start date: June 2006
Phase: Phase 2
Study type: Interventional

This is a randomized, dose-ranging, efficacy and tolerability study in chronic kidney disease patients with hyperphosphatemia on hemodialysis. Patient participation in the study is approximately 10 weeks in duration.