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Kidney Failure, Chronic clinical trials

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NCT ID: NCT00211978 Completed - Kidney Failure Clinical Trials

EPIC(Effect of PhosLo on Phosphorus Levels in Chronic Kidney Disease)

Start date: May 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if calcium acetate (PhosLo) can control serum phosphorus in pre-dialysis patients with moderate to severe impairment of kidney function.

NCT ID: NCT00211653 Completed - Kidney Failure Clinical Trials

Acetylcysteine in the Prevention of Renal Failure After Bypass Surgery

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

The purpose of this study is to determine if Acetylcysteine is effective in preventing renal failure associated with cardiac surgery

NCT ID: NCT00202345 Completed - Anemia Clinical Trials

Iron Sucrose in Stage 3/4 Kidney Disease

Start date: August 2004
Phase: Phase 3
Study type: Interventional

One of the complications of late stage kidney disease is the development of a low red blood cell count (anaemia/low haemoglobin concentration). The Australian Commonwealth government limits funding of medications (called erythropoietic stimulating agents) to those patients who have already developed anaemia. There is evidence supporting the beneficial effects of maintaining a higher haemoglobin in these patients. Higher haemoglobin can delay the onset of dialysis and reduce the development of heart enlargement. However, the administration of erythropoietic stimulating agents is not without risk, including a high financial burden, worsening of high blood pressure and a rare complication called pure red cell aplasia. Previous studies have shown that patients with chronic kidney disease require additional iron to maintain the production of red blood cells. Thus it would be timely to determine if the administration of iron sucrose to these patients can maintain a near normal haemoglobin concentration, without the need to start an erythropoietic stimulating agent and possibly delaying dialysis. Study Hypothesis: That administration of iron sucrose is superior to standard care in the prevention of anaemia in patients with stage 3 /4 kidney disease.

NCT ID: NCT00195481 Completed - Kidney Failure Clinical Trials

Study Evaluating Sirolimus in Kidney Transplant Recipients in India

Start date: April 2004
Phase: Phase 4
Study type: Interventional

To determine the safety of sirolimus tablets in renal allograft recipients in a postmarketing surveillance setting.

NCT ID: NCT00195468 Completed - Kidney Failure Clinical Trials

Study Comparing Cyclosporine Dose Reduction vs. Cyclosporine Elimination in Kidney Transplant Recipients Taking Sirolimus

Start date: March 2004
Phase: Phase 4
Study type: Interventional

Compare kidney function as measured by calculated creatinine clearance (using the method by Nankivell)1 at 12 months after transplantation in subjects receiving induction therapy with cyclosporine microemulsion (CsA) and Rapamune followed by CsA dose reduction (Group I) with subjects receiving induction therapy with CsA and Rapamune followed by CsA discontinuation (Group II).

NCT ID: NCT00195429 Completed - Kidney Failure Clinical Trials

A Study Comparing the Withdrawal of Steroids or Tacrolimus in Kidney Transplant Recipients

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

This study evaluates two different immunosuppression drug regimens in patients with a recent kidney transplant. Patients initially received a regimen of Sirolimus, Tacrolimus and Prednisone and then randomized to discontinue either Tacrolimus or Prednisone.

NCT ID: NCT00187629 Completed - Healthy Clinical Trials

Phosphate Intake's Effect on the Skeletal System - Pilot

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

The purpose of this study is to determine the effects of different amounts of phosphorus in the diet on hormones that control phosphorus and bone health both in men who are healthy and in ones who have moderate kidney disease.

NCT ID: NCT00183248 Completed - Clinical trials for Kidney Transplantation

Using Donor Stem Cells and Alemtuzumab to Prevent Organ Rejection in Kidney Transplant Patients

Start date: September 2004
Phase: Phase 1/Phase 2
Study type: Interventional

Alemtuzumab is a man-made antibody used to treat certain blood disorders. This study will evaluate treatment of kidney transplant recipients with alemtuzumab and other immune system suppressing medications with or without infusions of bone marrow stem cells from the kidney donor. The purpose of this study is to find out which strategy is more effective in preventing organ rejection and maintaining patient health.

NCT ID: NCT00172211 Completed - Clinical trials for Kidney Failure,Chronic

Comparison of Oxidative Stress and Insulin Resistance Before and After Using Physioneal in Peritoneal Dialysis Patients

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

Patients affected by end-stage renal disease (ESRD) are subjected to enhanced oxidative stress, as a result of reduced anti-oxidant systems and increased pro-oxidant activity. Besides, insulin resistance is also very common in ESRD patients. Both enhanced oxidative stress and insulin resistance increase the risk of atherosclerosis and cardiovascular mortality, and intention to reduce oxidative stress and insulin resistance is important in ESRD patients who suffer from high cardiovascular risk. The high concentration of glucose and glucose degradation products (GDP), high lactate, and low pH in conventional peritoneal dialysis (PD) solutions are known as bioincompatible factors, which are believed to increase oxidative stress in PD patients. Physioneal®, a more biocompatible dialysis solution with neutral pH, physiologic bicarbonate concentration and low GDP level, has been applied in Europe for several years. Previous studies of Physioneal® have revealed advantages of improved infusion pain, more efficient acid-base control, increased ultrafiltration, and reduced peritonitis duration. However, its effects on oxidative stress and insulin resistance in peritoneal dialysis patients are not reported yet. The comparison of oxidative stress and insulin resistance before and after using Physioneal® may help to elucidate the possibly beneficial effects on uremic patients, which frequently suffer from increased oxidative stress and insulin resistance. Thirty continuous ambulatory peritoneal dialysis (CAPD) patients will be selected in this study, and receive conventional solution (Dianeal® PD-2 or PD-4) for a baseline period of 3 months. Then Physioneal® will be used for 3 months. Clinical conditions, biochemical and hematological parameters, oxidative markers in blood and effluent, and insulin resistance will be measured at baseline, before and after Physioneal®, and some markers will be measured 1 month after discontinuing Physioneal® and changing back to conventional solution. The medication used in each patient will be recorded, and the dialysis prescription will be adjusted by a nephrologist according to clinical data. The data collected before and after Physioneal® will be analyzed by paired-t test.

NCT ID: NCT00167947 Completed - Kidney Failure Clinical Trials

Study Evaluating Sirolimus in Kidney Transplant Recipients.

Start date: January 2005
Phase: Phase 3
Study type: Interventional

Renal function at 12 months assessed by calculated creatinine clearance.