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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT01457001 Terminated - Clinical trials for Chronic Renal Failure

Clinical Trial on the Use of 25-OH -D Vitamin in Haemodialysis Patients

NUTRIVITA-D001
Start date: November 2012
Phase: Phase 3
Study type: Interventional

Multicentric randomized Italian clinical trial, open label, not for profit. To evaluate the efficacy of 25-OH-D vitamin in terms of myocardial infarction, stroke, sudden death, death for other causes in chronic haemodialysis patients. Two arms of treatment: 25-OH-D vitamin per os versus no treatment.

NCT ID: NCT01442402 Terminated - Clinical trials for Kidney Failure, Chronic

APOL1 Gene Variants in African American Kidney Transplant Recipients

Start date: April 2014
Phase:
Study type: Observational

Aim 1: Determine if there is an association between the APOL1 risk variants and allograft survival and function in African Americans Aim 2: Determine if there is an association between the presence of APOL1 risk variants in an African American kidney transplant recipient and the risk of recurrent disease Aim 3: Investigate mechanisms of APOL1 associated kidney disease by prospectively following African American kidney transplant recipients throughout their clinical course.

NCT ID: NCT01441570 Terminated - Hypertension Clinical Trials

The Impact of Nebivolol Versus Metoprolol on Quality of Life

Start date: February 2012
Phase: N/A
Study type: Interventional

In an open label analysis, nebivolol has been shown to have a positive impact on quality of life in the general hypertensive population. That is, patients treated with nebivolol reported less side effects compared to those treated with metoprolol. Also, more nebivolol treated patients reached normalization of blood pressure. Although there is no data, it is believed that the impact would be similar in renal transplant recipients. The primary goal of this study is to determine if nebivolol will improve the quality of life measurements of kidney transplant recipients as compared to those treated with metoprolol succinate. This will be measured by comparing the scores of four quality of life questionnaires taken before and after 12 weeks of treatment with study drug. Other aims of this study are to determine if the use of nebivolol is cost-effective in the renal transplant recipient; determine if there is a change in urine protein excretion and renal function with the use of nebivolol; and determine the number of patients that maintain or achieve a target blood pressure of ≤ 120/80 mmHg.

NCT ID: NCT01437943 Terminated - Clinical trials for Kidney Failure, Chronic

Effect of Short Term Aliskiren Treatment in Kidney Transplant Patients

Start date: April 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effect of a short-term aliskiren treatment on kidney metabolism in patients at high risk for developing kidney dysfunction (i.e. kidney transplanted patients). The study is aimed at evaluating if any effect on kidney metabolism [using proton MR Spectroscopy(1H-MRS)] can be detected following a 6 months treatment with aliskiren regardless of its anti-hypertensive role. 1H-MRS can record a larger number of chemical species (up to 40) in the kidney, and monitor changes according to the pathologic state and health of the transplanted kidney.

NCT ID: NCT01437761 Terminated - Renal Failure Clinical Trials

Sorbent Treatment Prescriptions Pilot Study

Sorb2
Start date: August 2011
Phase: N/A
Study type: Observational

This study will compare how well blood of renal failure patients is cleaned with the new 2008 Sorbent System using two different dialysate speeds.

NCT ID: NCT01392196 Terminated - Heart Failure Clinical Trials

Renal Denervation in Patients With Chronic Heart Failure & Renal Impairment Clinical Trial

SymplicityHF
Start date: October 2011
Phase: N/A
Study type: Interventional

This is a feasibility study enrolling up to 40 patients in Australia and Europe. The primary aim of the study is to demonstrate the renal denervation with the Symplicity Catheter is safe and determine the evidence of a response to renal denervation in patients with Heart Failure.

NCT ID: NCT01363921 Terminated - Clinical trials for Cardiovascular Disease

Effect of HCO1100 on Cardiovascular Function

HicoCARD
Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether high porous membranes are effective in the treatment of cardiovascular events in chronic dialysis patients.

NCT ID: NCT01359579 Terminated - Renal Impairment Clinical Trials

A Study of the Pharmacokinetics and Safety of Varespladib in Subjects With Normal or Impaired Renal Function

Start date: June 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare and evaluate the pharmacokinetic characteristics and the safety of varespladib methyl in mild or moderate renal impairment patients and healthy volunteers.

NCT ID: NCT01351675 Terminated - Clinical trials for Diabetes Mellitus, Type 2

Bardoxolone Methyl Evaluation in Patients With Chronic Kidney Disease and Type 2 Diabetes

BEACON
Start date: June 30, 2011
Phase: Phase 3
Study type: Interventional

This study assesses the efficacy of bardoxolone methyl relative to placebo in delaying progression to end-stage renal disease (ESRD) and cardiovascular deaths in patients with Stage 4 Chronic Kidney Disease (CKD) and type 2 diabetes receiving standard of care.

NCT ID: NCT01318811 Terminated - Heart Failure Clinical Trials

A Comparison of Dilute Versus Concentrated Heparin for CRRT Anticoagulation

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

Heparin is commonly used for anticoagulation of the extracorporeal circuit during continuous renal replacement therapy (CRRT) but the optimal mode of delivery has not yet been validated. Our study will compare dilute heparin to a standard concentration of heparin. The investigators hypothesize that heparin delivered in a dilute solution will augment coating of the filter fibers with anticoagulants, decreasing clotting events and increasing filter life. By improving delivery of heparin to the filter and circuit, where clotting events can disrupt dialysis, less heparin would be required for the extra-corporeal circuit and thus less heparin would be delivered back to the patient with blood return from the machine. By exposing the patient to less heparin it is hypothesized that fewer bleeding events would occur, making the dialysis treatment safer. If more of the filter's fibers remain patent and the filter is functional for a longer period of time, the CRRT would also be more effective.