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Hemodialysis clinical trials

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NCT ID: NCT00418366 Completed - Hemodialysis Clinical Trials

A Study on the Effect of Kidney Disease on a Diabetes Medication (0431-008)

Start date: January 2003
Phase: Phase 1
Study type: Interventional

A study to evaluate the effect of kidney disease, from mild to severe disease, on a diabetes medication

NCT ID: NCT00413803 Completed - Hemodialysis Clinical Trials

Comparison of Four and Eight Hours Dialysis Sessions in Thrice Weekly Hemodialysis

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

The investigators hypothesize that an increase in the duration of dialysis session in thrice weekly center hemodialysis may provide better outcome, less morbidity, higher quality of life, lesser requirement of medications, and lower total cost.

NCT ID: NCT00410449 Completed - Clinical trials for End Stage Renal Disease

Oxidative Stress and Hemodialysis Access Failure

Start date: May 2001
Phase: Phase 4
Study type: Observational

Complications of hemodialysis access are the most frequent single reason for hospitalization among patients with End Stage Renal Disease (ESRD). Uremia, and particularly uremia in patients with diabetes, is a state of increased oxidative stress. The central hypothesis to be tested by this project is that oxidative stress is a major (and modifiable) trigger for vascular access complications. We hope to slow or reduce rates of stenosis, thrombosis and access complications by giving Vitamin E supplementation to patients being treated by hemodialysis.

NCT ID: NCT00404456 Completed - Hemodialysis Clinical Trials

The Efficacy of Melatonin in Sleep Problems of Hemodialysis and Peritoneal Dialysis Patients

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

Sleep problems can lead to a bad quality of life and a raise of morbidity, also in dialysis patients. Sleep problems can be caused by a disturbance of circadian rhythms in our body. For a good regulation of these circadian rhythms a uniform external synchronisation is necessary. This is the synchronisation of the biological clock of our body by light and other influences. In case of a disturbance of the external synchronisation, due to for example naps during the day or wake periods at night, internal rhythms can be unlinked. As a result a weakened melatonin rhythm and a problematic sleep-wake cycle can be observed. Most dialysis patients have sleep problems. Their sleep latency is prolonged. They often take a nap during the day and their sleep efficiency is poor. There has only been one study on the melatonin rhythm of dialysis patients. The conclusion of this study was that the melatonin rhythm of dialysis patients is weakened and disturbed, probably caused by renal insufficiency. In this study no link was made between melatonin rhythm and the nature and severity of possible sleep problems. In different studies with non-dialysis patients and a disturbed melatonin rhythm, exogenous melatonin at the right time leads to a recovery of the normal rhythm and the normal biological clock and a better quality of life. The aim is to research the endogenous melatonin rhythm and to improve sleep problems of hemodialysis patients with a placebo-controlled study with exogenous melatonin. Next to this a substudy is performed, in which the effect of the change of daytime to nocturnal in hospital hemodialysis on sleep and melatonin is researched.

NCT ID: NCT00347490 Completed - Hemodialysis Clinical Trials

HENOX: Enoxaparine in Hemodialysis

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

Primary objective: To assess clinical efficacy of single bolus anticoagulation with Enoxaparin in chronic hemodialysis Secondary objective: To assess safety and tolerability by the number of spontaneously reported adverse events by patients

NCT ID: NCT00319774 Completed - Hemodialysis Clinical Trials

Hemocontrol and Blood Pressure Control in Dialysis Patients

Start date: December 2002
Phase: Phase 3
Study type: Interventional

Volume overload contributes significantly to the pathogenesis of hypertension in hemodialysis patients. The Hemocontrol(HC)system (Gambro), which automatically adjusts ultrafiltration rate and dialysate conductivity according to blood volume variations during dialysis, has been suggested to improve hemodynamic tolerance and thus facilitate fluid removal. This randomized controlled trial was designed to compare the use of HC with standard hemodialysis to test the hypothesis that the use of the HC system may lower home blood pressure in comparison with standard hemodialysis as a primary endpoint. Secondary endpoints are a variation in the percentage of dialysis sessions requiring nurses’ interventions for intra-dialytic hypotension and a change in the health-related quality of life of HD patients.

NCT ID: NCT00317005 Completed - Clinical trials for Cardiovascular Disease

Uremic Hyperhomocysteinemia -A Folate Trial for Possible Prevention of Cardiovascular Events

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

Homocysteine recently gained access to the category of risk factor for the development of atherosclerotic cardiovascular disease in the general population. Chronic renal failure patients, even before being introduced to dialysis therapy have almost universal elevation of serum homocysteine; when on dialysis their mortality is above 50% related to cardiovascular disease that we might now speculate, with a contribution of potentially toxic levels of the aminoacid homocysteine.

NCT ID: NCT00309348 Completed - Hemodialysis Clinical Trials

Ultrasound Instrument to Prevent Dialysis Graft Failure

Start date: February 27, 2006
Phase: N/A
Study type: Interventional

This research study aims to show that a newly developed investigational Doppler instrument can reliably measure blood flow in dialysis access grafts, to see if a decrease in the flow may be a sign of impending graft failure and also to see if there is evidence that by monitoring the flow in these grafts their lives may be extended. The new investigational device is to be known as FloMon; this is an ultrasonic device that provides blood flow measurements from a small probe placed in a noninvasive manner above the graft or blood vessel. The instrument is being developed so that it may help give insight to on-coming graft failure which may be prevented. The FloMon is an extension of a previously Food and Drug Administration (FDA) cleared instrument, Echoflow-A, which had been used in a similar study as this one. The Echoflow-A is similar to this device in all respects with the exception of design and calculation of measurement. The FloMon compared to the Echoflow-A is better ergonomically designed and reads flow readings in about 2 minutes versus twice the time necessary to take similar measurements using the Echoflow-A.

NCT ID: NCT00307996 Completed - Hemodialysis Clinical Trials

The Effect of CoQ10 Administration on Hemodialysis Patients

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

The purpose of this study is to examine whether CoQ10 administration is effective as an antioxidant in hemodialysis patients.

NCT ID: NCT00298441 Completed - Hemodialysis Clinical Trials

Efficacy of Intravenous Iron Administration in Hemodialysis Patients

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

The purpose of this study is to determine whether the frequency of intravenous iron administration has an effect on anemia correction and oxidative stress formation in hemodialysis patients.