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Proteinuria clinical trials

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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: NCT00801463 Completed - Proteinuria Clinical Trials

Prednisone Plus Tripterygium Wilfordii Treatment of Adult Patients With Idiopathic Focal Segmental Glomerulosclerosis

Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the efficacy of prednisone and tripterygium wilfordii in treated Focal Segmental Glomerulosclerosis (FSGS).

NCT ID: NCT00768638 Completed - Clinical trials for Chronic Kidney Disease

Study of Atorvastatin Dose Dependent Reduction of Proteinuria

SARP
Start date: October 2008
Phase: Phase 4
Study type: Interventional

Randomized controlled double blind study of parallel groups to evaluate the comparative effects of low-dose of atorvastatin on proteinuria in patients with stage 3 or 4 chronic kidney disease.

NCT ID: NCT00722215 Completed - Clinical trials for Chronic Kidney Disease

Endothelin Receptor Antagonism in Proteinuric Nephropathy

Start date: May 2006
Phase: Phase 1
Study type: Interventional

The number of people with kidney problems is increasing rapidly, related in part to the increasing prevalence of diabetes. Patients with kidney problems tend to have protein leaking into the urine (proteinuria). Both proteinuria and the kidney disease itself are associated with an increased risk of heart disease. Reducing proteinuria is an important treatment goal in people with kidney problems. Endothelin is a chemical produced both by blood vessels and the kidney. Higher than normal levels of endothelin are thought to contribute to progression of kidney disease and proteinuria. By using drugs that block the effects of endothelin ('endothelin receptor antagonists') we can hopefully reduce both of these. The purpose of the study is to ascertain whether endothelin receptor antagonists improve kidney function and reduce proteinuria more so than other commonly used drugs.

NCT ID: NCT00713011 Withdrawn - Hypertension Clinical Trials

Adalat XL vs Diltiazem on Proteinuria and Blood Pressure in Hypertensive Diabetic Patients

CARDINAL
Start date: November 2008
Phase: Phase 3
Study type: Interventional

The study consists of a 12 week run-in period when all subjects are stabilized on a single dose of Avalide (300 mg/12.5 mg or 300mg/25mg dose) per day. After this 12 week run-in ends, subjects will be randomly assigned to start the addition of either Adalat XL or Tiazac XC for 18 weeks of treatment. Subjects will have a 1 in 2 chance of receiving the study drug Adalat XL and a 1 in 2 chance of receiving the drug Tiazac XC. An end of treatment visit will be done 18 weeks after start of study drug. The expected duration of the study is 30 weeks. The purpose of this study is to compare the change in proteinuria, through a urine test, while taking study drug until high blood pressure (BP) is reduced to near normal levels in study subjects with diabetic nephropathy and hypertension.

NCT ID: NCT00698659 Terminated - Hypertension Clinical Trials

Pharmacodynamic Effects of Anti-Vascular Endothelial Growth Factor Therapy in Patients With Advanced Malignancies

Start date: August 2007
Phase: N/A
Study type: Observational

1. To determine the effect of anti-vascular endothelial growth factor (VEGF) on endothelial function and on retinal microvasculature 2. To determine endothelial dysfunction as a marker of early response and as an indicator for the development of hypertension and proteinuria in patients treated with anti-VEGF agents 3. To characterize the effect of anti-VEGF therapy on the pulmonary function of patients with malignancy (primary or secondary) involving the lung

NCT ID: NCT00674596 Completed - Diabetes Clinical Trials

The Effect of Renin Angiotensin System Blockage (RAS) Blockade On PTX3 Levels In Diabetic Patients With Proteinuria

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

Long pentraxin 3 (PTX3) is a recently discovered multimeric inflammatory mediator structurally linked to CRP and serum amyloid P-component. There is no data about the effects of Renin angiotensin system blockage (RAS) on PTX3 levels in diabetic patients with proteinuria. The aim of this study was to find out whether the beneficial effects of RAS blockage in diabetic proteinuria has any relation with the alteration of PTX3 levels. We searched for the effects of ACE inhibitor ramipril on the clinical and laboratory parameters of diabetic patients with proteinuria.

NCT ID: NCT00663949 Completed - Clinical trials for Diabetic Nephropathy

Assessment of the Effect of Captopril Versus Combination of Captopril and Pentoxifylline on Reducing Proteinuria in Type 2 Diabetic Nephropathy

Start date: February 2006
Phase: Phase 2/Phase 3
Study type: Interventional

Diabetic nephropathy is the most common cause of ESRD and has a great impact on mortality and morbidity of diabetic patients. Despite renoprotective effect of ACE inhibitors in diabetic patients they can not hinder the progression of renal disease completely. Pentoxifylline as a TNFa blocker may hinder progression of diabetic nephropathy in combination of captopril.

NCT ID: NCT00655330 Active, not recruiting - Clinical trials for Type 2 Diabetes Mellitus

Probucol Combined With Valsartan in Reducing Proteinuria in Diabetes Nephropathy

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

This is a prospective randomized controlled, open-labeled study to identify the efficacy of probucol in combination with valsartan in patients with Diabetes nephropathy. The reduction of urinary albumin or proteinuria will be the primary outcome studied. The expected study duration will be 48 weeks.

NCT ID: NCT00654771 Completed - Hypertension Clinical Trials

Comparison of Catheterized and Clean Catch Urine Specimens for Protein/Creatinine Ratio in Preeclampsia Evaluation

UPREE
Start date: July 2005
Phase: N/A
Study type: Observational

The purpose of this prospective study was to examine whether protein/creatinine ratios in catheterized urine specimens correlate to clean catch specimens in pregnant patients being evaluated for preeclampsia.