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Kidney Failure, Chronic clinical trials

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NCT ID: NCT00986947 Completed - Kidney Failure Clinical Trials

Desensitization of Highly Sensitized Deceased Donor Renal Transplantation Candidates

Start date: September 2009
Phase: Phase 2
Study type: Interventional

Some patients who need kidney transplants have high levels of antibodies that make them incompatible with most potential deceased donor kidney offers. These patients are considered highly-sensitized and are very difficult to transplant because the likelihood that they will receive a compatible organ is very low. There are some medications and procedures that can decrease the antibody levels and this can increase the chance of finding a compatible donor for these patients. In this study the investigators will give two medications (IVIg and Rituximab) to highly-sensitized patients who are on the waiting list for a deceased donor kidney transplant. After the investigators administer these medications, the investigators will continue to check for compatibility as organ offers are received. If a compatible organ offer is received, the investigators will perform the transplant using that organ. The investigators hypothesize that these medications will lower antibody levels and increase the chance that a these patients are able to receive a compatible kidney transplant.

NCT ID: NCT00982527 Completed - Clinical trials for Kidney Failure, Acute

Fenoldopam in Pediatric Cardiac Surgery

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether fenoldopam infusion during cardiopulmonary bypass in young children with congenital heart disease is able to reduce indicators of acute kidney injury (biomarkers reduction, diuresis increase) compared to a control group.

NCT ID: NCT00943995 Completed - Clinical trials for Kidney Failure, Chronic

Three Times Weekly (TIW) Growth Hormone Therapy in Children on Hemodialysis

Start date: July 2010
Phase: Phase 3
Study type: Interventional

Hypotheses: 1. The provision of thrice weekly subcutaneous (SQ) recombinant growth hormone (rGH) therapy to children receiving in-center hemodialysis (HD) will result in improved growth. 2. The provision of thrice weekly SQ rGH therapy to children receiving in-center HD will result in improved lean body mass, nutritional status and quality of life. TIW rGH treatment regimen (0.35 mg/kg/week divided into 3 doses, each dose being given at the conclusion of the dialysis treatment) for up to 2 years; growth response, Dual energy X-ray absorptiometry (DEXA), and quality of life (QOL) will be measured. The goal is to enroll 20 children who are Tanner 1 with decreased height SDS and/or decreased height velocity standard deviation scoreS (SDS). If this therapy is demonstrated to be efficacious and improves growth and QOL, this therapy could be easily implemented for all eligible children on HD, since parental acceptance should be better without having to administer the rGH at home and compliance for the child will be assured. The investigators thus propose an important study that has the ability to advance their understanding and provide evidence for the best methods to promote growth in children on dialysis. The results of this study will result in important information that will be of value to the entire pediatric nephrologist community, including health care professionals, patients, and families. In a real sense, this study will build on the 2006 Consensus Conference guidelines for evaluation and treatment of growth failure in children with chronic kidney disease (CKD). This will provide evidence for critical management decisions that can help insure better growth opportunities to more children with CKD.

NCT ID: NCT00926562 Completed - Clinical trials for Kidney Failure, Chronic

A Safety Comparison of Iopromide and Iodixanol in Renal Impaired Patients

DIRECT
Start date: February 2009
Phase: Phase 4
Study type: Interventional

The investigators intend to find out which contrast agent has less kidney toxicity in renal impaired patients undergoing cardiac angiography or percutaneous coronary intervention (PCI).

NCT ID: NCT00919438 Completed - Kidney Failure Clinical Trials

Non Invasive External Monitoring in Dialysis Patients

FARM
Start date: January 2009
Phase: N/A
Study type: Observational

This is a single center, non randomized study to gather data to correlate physiological signals with the patient's fluid status during fluid removal in hemodialysis.

NCT ID: NCT00912184 Completed - Shock Clinical Trials

Study Comparing High Cut-off Haemofiltration With Standard Haemofiltration in Acute Renal Failure

Start date: May 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This trial aims to study the effect of combining continuous and a new polyamide membrane with larger pores in the treatment of critically ill patients with acute renal failure and low blood pressure (shock) requiring noradrenaline. The investigators wish to compare the clinical effect of this new therapy to that of haemofiltration with a standard membrane.

NCT ID: NCT00908843 Completed - Clinical trials for KIDNEY FAILURE, ACUTE

Prevention of Contrast Induced Nephropathy (NIC) by Intravenous Versus Oral Rehydration

NIC
Start date: September 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the efficacy of oral versus intravenous hydration in the prevention of the contrast-induced nephropathy.

NCT ID: NCT00906204 Completed - Clinical trials for End-Stage Renal Disease

Safety Trial of Single Versus Multiple Dose Thymoglobulin Induction in Kidney Transplantation

STAT
Start date: March 2010
Phase: Phase 2
Study type: Interventional

In a non-blinded pilot study conducted at the University of Nebraska Medical Center, evidence was found that a single large dose of Thymoglobulin on the day of kidney transplantation produced better kidney function than the standard dosing plan, when the same amount is divided into smaller doses on 4 days. This new study repeats that dose comparison, but with double-blinding and at multiple transplantation centers.

NCT ID: NCT00875017 Completed - Clinical trials for Kidney Failure, Chronic

Comparing Absorption of Dietary Phosphorus When Administering FOSRENOL® or RENVELA® in Healthy Adult Volunteers

Start date: April 20, 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare the absorption of dietary phosphorus following a single dose with lanthanum carbonate (1000mg) and a single dose of sevelamer carbonate (2400mg).

NCT ID: NCT00853242 Completed - Clinical trials for Kidney Failure, Chronic

Randomized Study Comparing Genz-644470, Placebo, and Sevelamer Carbonate in Chronic Kidney Disease Patients on Hemodialysis

LEAP
Start date: February 2009
Phase: Phase 2
Study type: Interventional

The purpose of this clinical study is to compare the effects of Genz-644470 with the effects of placebo and sevelamer carbonate (Renvela®) on the reduction of serum phosphorus in hyperphosphatemic chronic kidney disease participants on hemodialysis.