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Hemodialysis clinical trials

View clinical trials related to Hemodialysis.

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NCT ID: NCT01400126 Not yet recruiting - Clinical trials for System as Compared to Conventional Water System.

Ultrapure Water System for Hemodialysis Therapy

Start date: August 2011
Phase: N/A
Study type: Observational

We wish to compare the effect of very clean water used for dialysis therapy (i.e ultrapure water) in comparison with the use of conventional water which are used in most dialysis units worldwide. To the best of our knowledge prospective data in that field is sparse.

NCT ID: NCT01371890 Completed - Hypertension Clinical Trials

Mechanisms and Treatment of Intradialytic Hypertension - Sodium

MATCH-Sodium
Start date: May 2011
Phase:
Study type: Observational

The purpose of this study is to determine the role of dialysate exposure and fluid removal during hemodialysis in the pathophysiology of intradialytic hypertension.

NCT ID: NCT01352455 Completed - Hemodialysis Clinical Trials

More Frequent In-Center Hemodialysis in Pediatric End Stage Renal Disease

Start date: March 2011
Phase: N/A
Study type: Interventional

A health kidney works 24 hours a day, 7 days a week to remove toxins and fluid from the body. Many children with permanent kidney failure undergo dialysis, a life saving procedure that takes the place of a kidney. Currently, many children with permanent kidney failure only receive dialysis treatments 3 days a week in the hospital dialysis clinic. Children on dialysis have a markedly reduced life expectancy, with a life span 40-50 years shorter than their healthy counterparts. Survival for these children has not improved over the last 20 years. These data indicate that the current dialysis treatment strategy is unacceptable. This research project will study if more frequent dialysis, performed 5 days per week, will improve the health of children with permanent kidney failure compared to the current treatment strategy. Children will be treated with both traditional and more frequent dialysis schedules to measure improvements in their health and well being.

NCT ID: NCT01341782 Completed - Hemodialysis Clinical Trials

Comparison of Efficacy and Safety of Paricalcitol Injection With Maxacalcitol Injection in Adult Japanese Chronic Kidney Disease Subjects Receiving Hemodialysis With Secondary Hyperparathyroidism

Start date: May 2011
Phase: Phase 3
Study type: Interventional

This study is a comparison of the efficacy and safety of paricalcitol injection with maxacalcitol injection in adult Japanese chronic kidney disease patients receiving hemodialysis with secondary hyperparathyroidism. The main objective of this study is to demonstrate the efficacy of paricalcitol injection in reducing levels of parathyroid hormone without clinically significant hypercalcemia, compared to maxacalcitol injection.

NCT ID: NCT01301027 Enrolling by invitation - Clinical trials for End Stage Renal Disease

Adipokines in Hemodialysis Patients

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

This is a double blinded RCT of pioglitazone vs. placebo in overweight or obese, diabetic and non-diabetic hemodialysis patients. This study will examine whether pioglitazone modulates adipokine production by adipose tissue in hemodialysis patients and whether these changes result in reduction of inflammation, insulin resistance and oxidative stress and increase in muscle mass. In addition, this study will also examine the associations of adiposity with adipokines and the metabolic milieu in hemodialysis patients to better understand the biology of adipocytes in uremic milieu.

NCT ID: NCT01271881 Recruiting - Hemodialysis Clinical Trials

Placement of Covered Stents to Treat Hemodialysis Access Stenoses in the Cephalic Arch and Central Veins

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

Balloon angioplasty is used to open up a narrowing that forms in hemodialysis fistula. Two areas of particular problems are the terminal portion of the cephalic vein near the shoulder and the central veins in the chest. Although angioplasty is standard of care the treated narrowed segments of vein mostly renarrow within 3 months requiring retreatment to keep your dialysis access functional. Recently there has been introduction of a new technology called a covered stent graft. Initial studies suggest that placing this device across the area of narrowing leads to dialysis access staying open longer and needing less angioplasty treatments. This study is designed to compare angioplasty (standard of care) versus using a covered stent graft. The investigators will then look at the dialysis records and future fistulograms to see if there is decreased flow through the fistula at 3, 6 and 12 months after the initial procedure.

NCT ID: NCT01269827 Completed - Inflammation Clinical Trials

Pentoxifylline and Systemic Inflammation in Hemodialysis Patients

Start date: January 2006
Phase: Phase 4
Study type: Interventional

The aim of this study was to compare the effect of PTX vs placebo on serum concentrations of TNF-α, IL-6, and CRP in patients on hemodialysis.

NCT ID: NCT01267617 Completed - Hypotension Clinical Trials

Measuring Cardiovascular Stress in Patients on Hemodialysis

Start date: November 30, 2010
Phase:
Study type: Observational

To determine if proprietary software that uses pulse-wave analysis to interpret the output of a conventional pulse-oximeter, can predict the onset of circulatory stress, before changes in blood pressure and pulse occur, in patients undergoing outpatient hemodialysis.

NCT ID: NCT01252823 Completed - Hemodialysis Clinical Trials

Implantable Loop Recorder in Hemodialysis Patients

RYTHMODIAL
Start date: December 28, 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to use implantable loop recorder (ILR) in patients under chronic hemodialysis to record arrhythmias and conduction disorders and correlate them with hemodialysis parameters.

NCT ID: NCT01252394 Unknown status - Hemodialysis Clinical Trials

Correspondence of ScO2 and Cardiac Output in Hemodialysis

Start date: November 2010
Phase: N/A
Study type: Observational

The study aims to investigate the correspondence between changes in central venous oxygen saturation (ScO2) and in cardiac output during hemodialysis. In 12 hemodialysis patients with an A-V fistula, a thoracic bioimpedance cardiograph will be validated for cardiac output measurements during ongoing hemodialysis. Provided this validation is satisfactory, impedance cardiography cardiac output and ScO2 will be measured at intervals during hemodialysis in 25 hemodialysis patients with a central vascular access. Absolute values and trends will be compared.