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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: NCT01770470 Completed - Clinical trials for End Stage Renal Disease

Chitosan Chewing Gum Study in Dialysis Patients

Start date: April 2010
Phase:
Study type: Observational

The purpose of the pilot study is to determine the impact of short-term administration of chitosan-containing chewing gum on phosphate levels in patients with elevated serum phosphate levels.

NCT ID: NCT01766882 Completed - Clinical trials for End Stage Renal Failure

Volume,Sodium and Blood Pressure Management in HD

VSBP
Start date: September 2012
Phase: N/A
Study type: Interventional

The purpose of this study to conduct a pilot, randomized trial in stable HD patients to evaluate the effect of gradual, step-wise reduction of post-hemodialysis target weight, combined with diligent dietary sodium restriction and reduction in dialysate sodium exposure on hydration/volume status and blood pressure (BP) control.

NCT ID: NCT01764854 Completed - Clinical trials for End Stage Renal Disease

Pharmacodynamic Study of AZD1722 in End-stage Renal Disease Patients on Hemodialysis

Start date: January 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the study drug is safe, tolerable and active in reducing fluid overload/weight gain between dialysis sessions for patients with End Stage Renal Disease on Hemodialysis.

NCT ID: NCT01756508 Completed - Clinical trials for End-Stage Renal Disease

Eculizumab for Prevention and Treatment of Kidney Graft Reperfusion Injury

Start date: September 1, 2012
Phase: Phase 2
Study type: Interventional

Study of eculizumab ability to correct the reperfusion injury of the kidney allograft.

NCT ID: NCT01729130 Completed - Clinical trials for Diabetes Mellitus, Type 2

Adipose Tissue Function After Pancreas Transplantation

Start date: September 2009
Phase:
Study type: Observational

Clinical measures of adipose tissue mass (BMI, waist circumference, waist-to-hip ratio) do not adequately explain the inter-individual and ethnic heterogeneity in diabetes. . There is a need to identify novel/universal markers of risk for diabetes (DM) and cardiovascular disease (CVD). These biomarkers also can become additional outcome measures for an intervention such as pancreatic/kidney transplant. If biological markers show an improvement with an intervention before anthropometric changes occur, intermediate outcomes can be an encouraging finding for practitioners. This study will focus on the central question of "adipose tissue dysfunction" as mediator of metabolic complications of positive energy balance, independent of body fat content and distribution. This study will address the question of effect of hyperglycemia on adipose tissue function independent of body fat mass. This project will take advantage of unique expertise of our investigators to perform detailed metabolic studies in patients with diabetes who undergo pancreatic/kidney transplant. The results of the proposed study will provide support to the novel approach of identifying adipose tissue dysfunction, rather than obesity and fat distribution, as predictor of diabetes and CVD across all ethnic groups, age and gender. We will obtain necessary preliminary data for future grant submissions to support our central hypothesis and develop stronger interactions within and outside The University of Texas Medical Branch (UTMB) with clinical investigators in the area of DM and its complications.

NCT ID: NCT01723111 Completed - Clinical trials for End-stage Renal Disease

Impact of Dialysis Modality on Hepcidin and Iron Metabolism

HERMES
Start date: November 2012
Phase: N/A
Study type: Observational

- Dialysis modality may influence the oxidative stress and proinflammatory cytokines in ESRD patients. - Dialysis modality may affect hepcidin - Dialysis modality may influence iron and ESA requirements.

NCT ID: NCT01710020 Completed - Hemodialysis Clinical Trials

Pharmacokinetics And Dialysability Of CP-690,550 In Subjects With End-Stage Renal Disease

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

There were 2 study periods in this study. In the Period 1, CP-690,550 was to be administered approximately 1 to 2 hours following hemodialysis. If significant non-renal clearance of the drug occurred such that dialyzability of CP-690,550 could not be assessed in Period 1, a second period (Period 2) will be conducted. In Period 2, a single dose of drug will be administered approximately 4 hours prior to hemodialysis.

NCT ID: NCT01698541 Completed - Clinical trials for End Stage Renal Disease

Generic Tacrolimus in the Elderly - Prograf® vs Tacni®

GenTac
Start date: February 2013
Phase: Phase 4
Study type: Interventional

Test bioequivalence of generic tacrolimus (Tacni), using original tacrolimus (Prograf) as comparator, in elderly (>60 yr) renal transplant recipients

NCT ID: NCT01689272 Completed - Clinical trials for End-stage Renal Disease

Functional Reserve Estimation of Donor Kidney

Start date: May 2011
Phase: Phase 4
Study type: Interventional

The purpose of the study: - To estimate the role of morphological, clinical, biochemical and imaging studies at stages of kidney transplantation (medical therapy, explantation, preservation, transplantation). - To improve the ways of preserving optimal functional parameters of renal transplants.

NCT ID: NCT01687699 Completed - Clinical trials for End-stage Renal Failure

Effects of Spironolactone on Cardio- and Cerebrovascular Morbidity and Mortality in Hemodialysis Patients

Start date: April 2008
Phase: Phase 4
Study type: Interventional

Aldosterone receptor blockers reduce cardiac-related morbidity and mortality. Recently, we demonstrated that long-term low-dose spironolactone is clinically safe in many hemodialysis (HD) patients. In the present study, we assess whether low-dose spironolactone treatment reduces the high incidence of cardio- and cerebrovascular (CCV) morbidity and mortality in HD patients. The investigators' hypothesis is that aldosterone receptor blockade by spironolactone reduces the risk of both CCV morbidity and death among HD patients.