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Renal Insufficiency, Chronic clinical trials

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NCT ID: NCT00823303 Completed - Clinical trials for Chronic Kidney Disease

Paricalcitol Versus Calcitriol for Efficacy and Safety in Stage 3/4 Chronic Kidney Disease (CKD) With Secondary Hyperparathyroidism (SHPT)

PACE
Start date: February 2009
Phase: Phase 4
Study type: Interventional

Secondary Hyperparathyroidism (SHPT) occurs in many patients with kidney disease and leads to bone disease. Active forms of vitamin D, calcitriol and paricalcitol, treat SHPT, but may have different effects on blood calcium. This study will randomize patients with SHPT and stage 3 or 4 CKD to treatment with calcitriol or paricalcitol, and monitor patients for the incidence of high blood calcium, and effectiveness of SHPT treatment.

NCT ID: NCT00821847 Completed - HIV Infections Clinical Trials

Renal Function Assessment in HIV Patient

HIVERS
Start date: June 2009
Phase: N/A
Study type: Observational

Recent progress in antiretroviral therapy has turned HIV infection into a chronic disease. Patients survival has dramatically improved but complications may occur that need to be prevented and monitored. As much as 10 % of HIV patients may suffer from chronic kidney disease, an affection that is not symptomatic until a very late stage secondary to HIV infection, drugs exposure, hypertension or diabetes. Guidelines have suggested that renal function should be regularly assessed in HIV patients to perform early diagnosis for chronic kidney disease and allow initiation of preventive measures aimed at preserving renal function. Plasma creatinine dosage is the easiest way to evaluate renal function but glomerular filtration rate estimation from cockcroft or MDRD formulae is a much better indicator of renal function. Other markers like cystatin C may be used. None of these markers has been validated in HIV patients. Therefore our study is aimed at comparing validity of creatinine clearance estimation with Cockcroft and Gault and MDRD formula and cystatin C compared to the gold standard measurement of glomerular renal function.

NCT ID: NCT00818792 Completed - Clinical trials for Chronic Kidney Disease

Randomized Comparison of xiEnce and visioN Coronary Stents in the sAme muLtivessel Patient With Chronic kiDnEy diSease

RENAL-DES
Start date: January 2009
Phase: Phase 2
Study type: Interventional

Percutaneous coronary intervention (PCI) with bare metal stent (BMS) in patients with renal insufficiency has shown unsatisfactory results. Indeed, drug-eluting stents (DES) might reduce the incidence of restenosis and therefore of target lesion revascularization procedures in these patients. We therefore designed a prospective, randomized, multicenter, not-sponsored study to directly compare the efficacy in the prevention of clinical restenosis of everolimus-eluting stent (Xience V) and bare-metal stent (Vision) (both 2nd-generation DES and BMS, respectively), both implanted in the same patient with multivessel disease and renal insufficiency in order to obviate for the multiple and unpredictable characteristics of this high-risk population.

NCT ID: NCT00817674 Completed - Clinical trials for Chronic Kidney Disease

Sleep Disturbances as a Non-traditional Risk Factor in CKD-Actigraphy

CRIC
Start date: November 2007
Phase: N/A
Study type: Observational

To test if usual at home night time sleep duration as measured with activity monitors and questionnaires will predict changes in kidney function as measured by kidney filtration rate and of cardiovascular function as measured by C-reactive protein in the blood. The study will explore the role of decreased sleep time or decreased sleep quality as a non-traditional risk factor for the progression of CKD and for the development of cardiovascular disease in CKD.

NCT ID: NCT00817492 Completed - Clinical trials for Chronic Kidney Disease

Sleep Disturbances as a Non-Traditional Risk Factor in Chronic Kidney Disease- University of Illinois

CRIC
Start date: July 2006
Phase: N/A
Study type: Observational

This study will help determine the relationship between impaired sleep and chronic kidney disease, specifically to determine if sleep disturbances are a risk factor for worsening kidney function.

NCT ID: NCT00817427 Completed - Clinical trials for Chronic Kidney Disease

Sleep Disturbances as a Risk Factor in Chronic Kidney Disease

CRIC
Start date: October 2008
Phase: N/A
Study type: Interventional

This study is designed to determine if either short night time sleep or poor night time sleep could be a risk factor for increasing the rate at which kidney function deteriorates in persons with mild to moderate kidney disease.

NCT ID: NCT00812123 Completed - Clinical trials for Chronic Kidney Disease

Calcineurin Free Immunosuppression in Renal Transplant Recipients

Start date: January 2001
Phase: Phase 4
Study type: Interventional

The main purpose of this study is to obtain preliminary information on the efficacy, safety and cost of two regimens, Rapamycin / MMF / steroid therapy and Cyclosporine A Neoral / MMF / steroid therapy, used in the prevention of acute rejection following renal transplantation.

NCT ID: NCT00811889 Completed - Type 2 Diabetes Clinical Trials

Trial to Determine the Effects of Bardoxolone Methyl on eGFR in Patients With Type 2 Diabetes and Chronic Kidney Disease

Start date: April 30, 2009
Phase: Phase 2
Study type: Interventional

This study assesses the effects of bardoxolone methyl (RTA 402) in patients with type 2 diabetes and chronic kidney disease.

NCT ID: NCT00810732 Completed - Clinical trials for Chronic Kidney Disease

Effects Of Sitaxsentan On Proteinuria, 24-Hour Blood Pressure, And Arterial Stiffness In Chronic Kidney Disease Subjects

FCRD01
Start date: May 9, 2007
Phase: Phase 2
Study type: Interventional

This study is being conducted to evaluate sitaxsentan dosing in subjects with chronic kidney disease.

NCT ID: NCT00808795 Completed - Diabetes Mellitus Clinical Trials

Efficacy of N-Acetylcysteine in Prevention of Post-Catheterization Contrast-Induced Nephropathy in Diabetic Patients With Chronic Kidney Disease

Start date: April 2006
Phase: Phase 3
Study type: Interventional

- Contrast-induced nephropathy (CIN) is the third most common cause of hospital acquired acute kidney injury, accounting for 10% of all cases. - The pathophysiology of CIN is unclear. Possible mechanisms involve 1. Renal tubular injury by oxygen free radicals 2. Reducing renal blood flow which leads to acute tubular necrosis. Since N-acetylcysteine is an antioxidant as well as a vasodilator, it may work in two distinct ways, by preventing reduction in renal blood flow or contrast-induced oxidative damage. - The purpose of this study is to evaluate the efficacy of N-acetylcysteine compared to placebo for the contrast-induced nephropathy prevention.