Clinical Trials Logo

End Stage Renal Disease clinical trials

View clinical trials related to End Stage Renal Disease.

Filter by:

NCT ID: NCT00614679 Completed - Clinical trials for End-Stage Renal Disease

A Novel Catheter Lock Solution for Treatment of Tunneled Hemodialysis Catheter-Associated Bacteremia

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

The primary objective is to investigate the ability of systemic intravenous antibiotic plus antibiotic/anti-biofilm (i.e. N-acetylcysteine) lock catheter technique in eradicating uncomplicated catheter associated bacteremia and salvaging the infected vascular catheter. Secondary objectives include duration to clearance of bacteremia, future recurrence of bacteremia, need for catheter removal and death.

NCT ID: NCT00608283 Completed - Clinical trials for End Stage Renal Disease

Live Kidney Donor Study

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

Kidney transplants from living donors now account for 40% of all the kidney transplants done in the United States. However, the current information on how donating a kidney can affect the donor's long term health needs further investigation. The purpose of this study is to collect data on a large number of live kidney donors and create and analyze a comprehensive database. Information about the number of living kidney donors, including those who have experienced kidney failure, heart problems, and death will be gathered for the database. Investigators will then use the database to identify the risks of kidney failure, associated conditions, and death after living donation. The database will also be used to identify characteristics that put donors at higher risk for health problems after donation.

NCT ID: NCT00604565 Terminated - Clinical trials for End Stage Renal Disease (ESRD)

Delivery of Soluble Ferric Pyrophosphate (SFP) Via the Dialysate to Maintain Iron Balance in Hemodialysis Patients

Start date: January 2008
Phase: N/A
Study type: Interventional

In maintenance hemodialysis patients, regular administration of parenteral iron by addition of soluble ferric pyrophosphate (SFP) to the dialysate, when compared to conventional dialysate, is effective in preventing the development of iron deficiency, thereby maintaining hemoglobin level; is clinically safe and does not lead to oxidative stress or inflammation.

NCT ID: NCT00597103 Completed - Clinical trials for Chronic Kidney Disease

Comparison of Dialysis Therapies on Cognitive Function

Start date: December 2007
Phase:
Study type: Observational

This study will evaluate the effects of more frequent dialysis on cognitive function including the assessment of sleep apnea and restless legs. Our hypothesis is that more frequent dialysis improves cognitive function and may have important implications on clinical care of ESRD patients and help to emphasize the need for treatments that will allow patients to live "with dialysis" rather than live "for dialysis".

NCT ID: NCT00597025 Completed - Clinical trials for End Stage Renal Disease

Impact of Providing High Protein Bar to Dialysis Patients With Low Serum Albumin

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

This study is to evaluate the impact of providing high protein supplementation in the form of a medical food bar containing 20grams of protein eath to hypoalbuminemic dialysis patients.

NCT ID: NCT00596167 Completed - Clinical trials for End Stage Renal Disease

Intradialytic Drug Removal by Short-daily Hemodialysis

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

Short-daily hemodialysis is increasingly becoming a preferred alternative to the conventional intermittent (three times per week) hemodialysis schedule. Studies have shown that short-daily dialysis improves a patient's quality of life, high blood pressure, anemia and calcium-phosphorus balance. Infection, however, will likely remain a persistent problem for dialysis patients regardless of the frequency of treatments. There is currently a wealth of information to guide doctors on how much and how frequently to give an antibiotic for patients who receive intermittent (thrice weekly) hemodialysis. However, there is very little information on how to prescribe antibiotics for patient's receiving short-daily hemodialysis. This study will develop drug dose guidelines for patients receiving short-daily hemodialysis for three frequently used antibiotics, vancomycin, levofloxacin and gentamicin. These guidelines will assist doctors so that patients receive the most effective dose and frequency of an antibiotic to treat their infection. The following is the study hypothesis which will be tested with two-sided, one sample t-tests comparing the AUC observed to historical measures8. 1) Vancomycin, levofloxacin and gentamicin are removed to a greater extent by short-daily hemodialysis than intermittent hemodialysis. The following are the specific aims: 1. Determine the interdialytic pharmacokinetics of vancomycin, gentamicin, and levofloxacin by short-daily HD. 2. Determine the extent of vancomycin removal when administered during the last hour of short-daily HD. 3. Develop drug-dosing guidelines for vancomycin, gentamicin and levofloxacin for patients receiving short-daily HD.

NCT ID: NCT00592618 Not yet recruiting - Sleep Apnea Clinical Trials

Effect of NAC on Sleep Apnea

Start date: n/a
Phase: N/A
Study type: Interventional

Sleep studies in ESRD patients have identified increased prevalence of Sleep Apnea. Based on current knowledge, treatment aimed at reducing oxidative stress might improve Sleep Apnea in HD patients. The aim of our study is to investigate the effect of N-acetylsysteine on Sleep Apnea in HD patients.

NCT ID: NCT00586716 Terminated - Clinical trials for End Stage Renal Disease

Intravenous Immune Globulin (IVIG) Treatment Protocol in Kidney Transplant Patients

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

The purpose of this study is to test the clinical and laboratory observations of IVIG therapy in the highly sensitized patient. We will study the effects of patients treated with IVIG or Cytogam in combination with plasmaphoresis to modulate the immune response in highly sensitized patients. The goal is to convert a positive crossmatch to a compatible crossmatch that would allow living related transplant to take place or to shorten time on the transplant waiting list.

NCT ID: NCT00586131 Completed - Clinical trials for End-stage Renal Disease

Arterial pH and Total Body Nitrogen Balances in APD

Start date: September 2003
Phase: Phase 4
Study type: Interventional

This study will test the hypothesis that by slightly lowering the acidity of blood (or increasing the pH), dialysis patients utilize protein and amino acids more efficiently.

NCT ID: NCT00580762 Terminated - Obesity Clinical Trials

Bariatric Surgery for ESRD Patients vs Control

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

This study will address a true clinical problem by developing a risk/benefit analysis for rapid surgical weight loss in the ESRD population. The risks of surgical intervention, as well as, potential nutritional concerns, balanced with that of the potential medical benefits associated with significant weight loss.