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End Stage Renal Disease clinical trials

View clinical trials related to End Stage Renal Disease.

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NCT ID: NCT00951977 Completed - Clinical trials for End Stage Renal Disease

Live Kidney Donor Study - Cross-Sectional and Historical Cohort Study

Start date: October 2009
Phase: N/A
Study type: Observational

Kidney transplantation from living donors has been shown to carry many benefits over deceased donor transplantation. Because of benefits such as shorter waiting times and improved outcome for transplant recipients, living kidney donation accounts for an increasing number of kidney transplants nationwide. Most published studies about living kidney donation demonstrate that the procedure is safe, but they also emphasize concerns that long-term data on live donor outcomes are insufficient. The purpose of this study is to assess the long term outcomes and risks that may arise from living kidney donation.

NCT ID: NCT00951353 Completed - Clinical trials for End Stage Renal Disease

Immune Development in Pediatric Transplantation (IMPACT)

Start date: July 2009
Phase:
Study type: Observational

Transplantation is the preferred method of treatment for end-stage renal disease (ESRD) in children. Over the past forty years, the use of newer immunosuppressive drugs has decreased the risk for organ rejection considerably, and improved short-term outcomes. However, these costly and complicated life-long treatment regimens also cause serious side effects. This has been particularly true for children, who undergo treatment with these drugs at the same time they are transitioning, physically and emotionally, from childhood to adulthood. These factors lead to significantly reduced life-spans, decreased drug regimen adherence, and an increased need for re-transplantation, as compared with adults. Current immunosuppressive procedures and strategies for children mimic those for adults, despite the difference between the two populations' immune systems and needs. New strategies aimed at tailoring to an individual child's needs would both reduce the risk of complications and improve outcomes. The purpose of this study is to generate information which will help to change the current practice of pediatric transplantation into one that is more individualized and preventative.

NCT ID: NCT00942253 Completed - Clinical trials for End Stage Renal Disease

Exercise Training in Dialysis Patients With Restless Legs Syndrome (RLS)

HDRLS
Start date: September 2006
Phase: Phase 2
Study type: Interventional

Uremic etiology Restless legs syndrome (RLS) has been associated with poorer quality of life (QoL) compared to RLS-free counterparts mainly due to sleep deprivation factors. Exercise training in hemodialysis (HD) patients with RLS has been proven to be a safe approach in temporally ameliorating RLS symptoms similarly to the use of pharmacological treatment with dopamine agonists. However it not known whether the exercise anabolic stimulus and the dopamine agonist treatment could act synergistically for the improvement of physical functioning and muscle performance as well as in the amelioration of augmentation symptoms in hemodialysis patients with RLS.

NCT ID: NCT00939952 Completed - Clinical trials for End Stage Renal Disease

Ertapenem Pharmacokinetics in Patients in Continuous Ambulatory Peritoneal Dialysis

Start date: June 2009
Phase: Phase 4
Study type: Interventional

The objective of this study is to characterize the pharmacokinetic profile of ertapenem during continuous ambulatory peritoneal dialysis (CAPD).

NCT ID: NCT00939445 Completed - Clinical trials for End Stage Renal Disease

Short Daily Hemodialysis and Online HDF: Which One is Better?

SHD
Start date: June 2009
Phase: Phase 3
Study type: Interventional

1. To compare the efficacy of 1. Short Daily Hemodialysis 2. Online HDF in term of adequacy of dialysis.

NCT ID: NCT00922701 Completed - Clinical trials for End-Stage Renal Disease

L-Carnitine in Peritoneal Dialysis

Start date: June 2004
Phase: Phase 2
Study type: Interventional

The development of glucose-sparing strategies able to provide an efficacious ultrafiltration profile represents one of the modern goals of peritoneal dialysis therapy. The study hypothesis is to evaluate the possibility to formulate peritoneal dialysis solutions containing L-carnitine as an osmotic agent to partially replace glucose.

NCT ID: NCT00912821 Completed - Clinical trials for End-stage Renal Disease

Effect of Different Dialysis Dosage on Prognosis in Maintenance Peritoneal Dialysis Patients

Start date: March 2009
Phase: Phase 4
Study type: Interventional

Peritoneal dialysis (PD) is an important model of renal replacement therapy for end-stage renal disease (ESRD) patients. Thus far, evidence for the initiation dosage of PD treatment is lacking, most patients begin their PD with four 2 L exchanges per day. However, many patients have their residual renal function at the initiation of PD, an 8 L dialysate per day will enhance the toxicity of bioincompatible dialysate and increase the economic burden compared with that of 6 L dialysate per day. Thus, the investigators perform a prospective, randomized, controlled, multi-center clinical study. The patients initiation of PD treatment within 6 months are randomized to be assigned to two groups: 6 L of dialysate per day and 8 L of dialysate per day, follow up will be regularly performed until 96 weeks. Clinical outcomes such as mortality, complications and life quality between the two groups will be investigated.

NCT ID: NCT00912782 Completed - Clinical trials for End-stage Renal Disease

Vitamin D and Arteriovenous Fistulae

Start date: January 2009
Phase: N/A
Study type: Interventional

Patients requiring hemodialysis following kidney failure need a form of dialysis vascular access in order to undergo the dialysis procedure. Dialysis vascular access dysfunction is an enormous clinical problem. While the best form of vascular access is the arteriovenous fistula (AVF), its primary problem is early, aggressive cellular ingrowth that leads to poor maturation of the vessel, preventing its use for dialysis. Strategies to prevent AVF failure are needed. Vitamin D is a hormone present in all human bodies and is important for good bone formation and immune function. There is new information that links vitamin D to the function of our veins and arteries, which are used in the creation of an arteriovenous fistulae. Our bodies can make vitamin D and can also get vitamin D from our diet. However, a majority of patients with chronic kidney disease and end-stage renal disease (ESRD) have low vitamin D levels (vitamin D deficiency). There are several benefits to correcting low vitamin D levels, however, it is not know whether correcting low vitamin D in the body will lead to better function of the vein and artery used for arteriovenous fistulae creation. The main goal of this pilot study is to examine the role of vitamin D supplementation on AVF maturation and useability for dialysis. Study results will be used to develop larger studies to examine the specific effect that vitamin D supplementation has on the vessels used for AVF creation and whether vitamin D promotes AVF maturation.

NCT ID: NCT00908297 Completed - Clinical trials for Cardiovascular Disease

Safety and Tolerability of Coenzyme Q10 in Hemodialysis Patients

Start date: February 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the safety and tolerability of the dietary supplement Coenzyme Q10 in hemodialysis patients.

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.