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Kidney Failure, Chronic clinical trials

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NCT ID: NCT00664066 Terminated - Anemia Clinical Trials

DELFT (Dynepo Evaluation of Long-Term Follow-Up Treatment)

DELFT
Start date: April 25, 2008
Phase:
Study type: Observational

This is a post-authorisation safety study to assess the incidence and severity of all pre-defined cardiovascular events in patients treated with DYNEPO, as well as to detect & describe less common adverse drug reactions, and to summarise DYNEPO drug utilisation.

NCT ID: NCT00654992 Completed - Clinical trials for Kidney Failure, Acute

Effect of Erythropoietin (EPO) in Kidney After Cardiac Surgery

EPO-CABG
Start date: September 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether erythropoietin is effective in preventing acute kidney dysfunction after coronary artery bypass grafting surgery.

NCT ID: NCT00645658 Completed - Kidney Diseases Clinical Trials

Testosterone Replacement Therapy in Advanced Chronic Kidney Disease

Start date: August 2007
Phase: N/A
Study type: Interventional

Muscle wasting is common in advanced chronic kidney disease (CKD) and adversely affects morbidity and mortality. In 2/3 of males with advanced CKD serum testosterone (TT) levels are reduced, and likely contributes to the wasting. As TT in relatively safe physiologic replacement doses, increases muscle mass in otherwise normal TT deficient subjects, we hypothesize that physiologic TT replacement will be effective in preventing and treating the loss of muscle mass and function in CKD patients, will improve quality of life and may reduce some cardiovascular disease (CVD) risk factors.

NCT ID: NCT00633308 Withdrawn - Kidney Failure Clinical Trials

Phosphorus and Calcium Removal During Long Hemodialysis Treatment Sessions

hemodialysis
Start date: March 2008
Phase: Phase 2
Study type: Interventional

The purpose of this sudy is to determined the effect of dialysate volume and treatment time on phosphate and calcium removal in stage V chronickidney disease patients treated by hemodialysis using the System One (NxStage Medical, Lawrence, MA)

NCT ID: NCT00629122 Completed - Clinical trials for Kidney Failure, Chronic

Pharmacokinetics of Sublingual Versus Oral Tacrolimus in Patients Awaiting Kidney Transplantation

Start date: February 2008
Phase: Phase 4
Study type: Interventional

Tacrolimus (Prograf) belongs to a class of medications known as the calcineurin inhibitors. It is a maintenance drug that is used to prevent rejection in kidney, liver, and heart transplant recipients. Calcineurin inhibitors display high pharmacokinetic (the body's effects on a drug) variability and necessitate use of blood tests to ensure that adequate drug levels are present to maintain effectiveness and safety. Early after transplant or at times when tacrolimus cannot be taken by mouth, alternative routes of administration are sought. Although an intravenous (through the vein) product is available, it can be toxic to the kidneys and has been associated with allergic reactions. Drug delivery via the oral mucosa is an alternative method of systemic drug administration which offers an alternative when oral administration is impractical (gastrointestinal dysmotility, reduced drug absorption, intestinal failure, difficulty in swallowing, or in those with nausea or vomiting). Administration of tacrolimus by the sublingual route may allow for direct entry into the systemic circulation and bypasses problems associated with drug absorption and breakdown that take place in the small intestine.

NCT ID: NCT00599391 Active, not recruiting - Kidney Failure Clinical Trials

Far Infrared Treatment for Kidney Diseases

Start date: February 2008
Phase: Phase 1
Study type: Interventional

Renal failure or kidney failure is a situation in which the kidneys fail to function adequately. It is divided into acute and chronic forms; either form may be due to a large number of other medical problems.

NCT ID: NCT00583765 Completed - Clinical trials for Kidney Failure, Acute

Evaluation of a Simplified Protocol for Regional Citrate Anticoagulation in Continuous Venovenous Hemodiafiltration

Start date: April 2005
Phase: N/A
Study type: Observational

Dialysis requires thinning of the blood to prevent clotting in the dialysis machine. Thinning of the blood is necessary but some forms of blood thinners may cause bleeding. Therefore, researchers are seeking ways to minimize bleeding risks and ensure effective dialysis. One medication used to thin the blood in the dialysis machine is citrate. Citrate has the advantage of having its blood-thinning properties quickly reversed by calcium in the patient's blood. As a consequence, only the blood in the machine is thinned, greatly reducing the risk of bleeding when dialysis is carried out using other blood thinners. Until now, most patients who received citrate for dialysis were administered the citrate in a separate infusion through an IV pump into the dialysis machine. This method requires complex monitoring and calculations. This study is about Prismocitrate which is a dialysis fluid very similar to the regular dialysis fluid that is used in this intensive care unit, except that this fluid already contains exactly the correct amount of citrate. Thus, this method does not require a separate pump for citrate and calculations to pump the citrate into the blood as it goes through the kidney machine. Having the citrate already contained in the dialysis fluid simplifies the procedure and reduces the possibility of calculation errors. This study seeks to determine if this simplified means of providing blood thinning in the kidney machine also results in the correct balance of blood salts.

NCT ID: NCT00563446 Completed - Anemia Clinical Trials

Study of the Efficacy of Darbepoetin Alfa in the Treatment of Renal Anemia

Start date: July 2005
Phase: N/A
Study type: Interventional

Anaemia is a common consequence of chronic renal failure. Darbepoetin alfa is a unique erythropoietic protein that stimulates erythropoiesis by the same mechanism as endogenous erythropietin and conventional recombinant human erythropoietin (rHuEPO). Darbepoetin alfa has been shown to have a serum half-life 3-fold longer than that of rHuEPO, which allows dosing at extended intervals and less frequent injection. The objective is to evaluate the efficacy and safety of darbepoetin alfa therapy given at an extended once monthly dosing interval in the treatment of renal anaemia in continuous ambulatory peritoneal dialysis.

NCT ID: NCT00556491 Completed - Clinical trials for Kidney Failure, Acute

Minocycline to Prevent Acute Kidney Injury After Cardiac Surgery

Start date: December 2007
Phase: N/A
Study type: Interventional

This study proposes to investigate whether treatment with minocycline pre-operatively in patients with mild to moderate chronic kidney disease undergoing cardiac surgery will reduce the occurence of kidney injury.

NCT ID: NCT00551655 Completed - HIV Infections Clinical Trials

Impact of Drug Therapy and Co-Morbidities on the Development of Renal Impairment in HIV-Infected Patients

Start date: May 2007
Phase: Phase 4
Study type: Observational

Tenofovir (TDF)-containing regimens may be associated with decreasing renal function in HIV-infected patients concurrently treated with boosted PI's and/or have co-morbid conditions including diabetes mellitus, hypertension, anemia, hepatitis B, and hepatitis C.