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Proteinuria clinical trials

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NCT ID: NCT00572663 Completed - Clinical trials for Chronic Kidney Disease

Optimalization of Nephroprotection Using N-Acetylcysteine

Start date: January 2005
Phase: N/A
Study type: Interventional

The main purpose of the study is find whether the addition of N-acetylcysteine (antioxidant) to dual renin-angiotensin-aldosterone system blockade involving angiotensin converting enzyme inhibitor and AT-1 angiotensin II receptor blocker leads to the reduction of proteinuria, main prognostic marker of chronic kidney disease progression.

NCT ID: NCT00572312 Completed - Clinical trials for Chronic Kidney Disease

Optimalization of Nephroprotection Using Atorvastatin (Sortis)

Start date: February 2005
Phase: N/A
Study type: Interventional

The main purpose of the study is find whether the addition of statin (Atorvastatin) to dual renin-angiotensin-aldosterone system blockade involving angiotensin converting enzyme inhibitor and AT-1 angiotensin II receptor blocker leads to the reduction of proteinuria, main prognostic marker of chronic kidney disease progression.

NCT ID: NCT00568178 Completed - Proteinuria Clinical Trials

An Extension Study Designed to Assess Effects of Losartan on Proteinuria in Pediatric Populations (MK-0954-326 AM1,EXT1(AM2))

Start date: June 1, 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effects of losartan on proteinuria in pediatric patients.

NCT ID: NCT00565396 Active, not recruiting - Proteinuria Clinical Trials

Effectiveness Study on Fosinopril and/or Losartan in Patients With Chronic Kidney Disease Stage 3

FLIP
Start date: September 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether fosinopril and losartan are effective in the treatment of patients with Chronic Kidney Disease(CKD) stage 3.

NCT ID: NCT00550095 Completed - Proteinuria Clinical Trials

To Assess the Effects of Valsartan on Albuminuria/Proteinuria in Hypertensive Patients With Type 2 Diabetes Mellitus

Start date: June 2007
Phase: Phase 4
Study type: Interventional

This study is designed to assess the efficacy of the different dosage forms of Valsartan[80, 160, and 320 mg] in reducing microalbuminuria/proteinuria in hypertensive patients with type 2 diabetes.

NCT ID: NCT00541619 Withdrawn - Hypertension Clinical Trials

Sympathetic Overactivity in Essential Hypertension

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

The primary objective of the study is whether subjects with hypertension and proteinuria display increased sympathetic nerve activity compared to hypertensive subjects without proteinuria and normotensive controls.

NCT ID: NCT00528385 Completed - Clinical trials for Chronic Kidney Disease

Optimalization of Nephroprotection Using Agents Inhibiting Renin-Angiotensin-Aldosterone System

Start date: March 2005
Phase: N/A
Study type: Interventional

The main purpose of the study is find whether the addition of aldosterone antagonist, spironolactone to dual renin-angiotensin-aldosterone system blockade involving angiotensin converting enzyme inhibitor and AT-1 angiotensin II receptor blocker leads to the reduction of proteinuria, main prognostic marker of chronic kidney disease progression.

NCT ID: NCT00524992 Completed - Proteinuria Clinical Trials

Evaluation of Albuminuria HIV-Infected Patients

Start date: August 29, 2007
Phase:
Study type: Observational

This study will examine the following: 1) how common albuminuria and proteinuria are among HIV-positive patients, 2) what causes albuminuria or proteinuria in these patients and 3) whether the condition becomes more severe over time. HIV-infected people are more likely than others to develop kidney disease. The earliest indicator of the possible presence of kidney disease is albuminuria (increased amounts of the protein albumin in the urine). A later indicator is the appearance of other proteins, a condition called proteinuria. HIV-infected patients 8 years of age and older who do not have diabetes, chronic kidney disease or cancer may be eligible for this study. Participants provide a urine sample during three visits as follows: the first upon enrollment in the study, a second 3 months later, and a third about 6 months after that. Blood samples are drawn at the first and last visits. At the first visit a medical history is taken and blood pressure, height, weight, waist circumference, hip circumference and upper arm skin thickness are measured. Participants who are found to have albuminuria or proteinuria are asked to undergo a kidney biopsy for research purposes. The procedure is optional. Participants who develop heavy proteinuria may be recommended to undergo a kidney biopsy in order to determine the nature of the kidney disease and begin treatment. The biopsy requires a 2-day hospital stay. For the procedure, an anesthetic is given to numb the skin and a needle is inserted and guided into the kidney to withdraw a small tissue sample. The needle is passed twice, and possibly three times. Following the procedure, the subject remains in bed rest for at least 10 hours to minimize the risk of excessive bleeding.

NCT ID: NCT00508898 Withdrawn - Clinical trials for Systemic Lupus Erythematosus

The Efficacy and Safety of Calcitriol for the Treatment of Lupus Nephritis and Persistent Proteinuria

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

Glomerulonephritis and renal failure represent one of the most life-threatening manifestations of systemic lupus erythematosus (SLE). Although immunosuppressive therapy is often effective for the treatment of acute lupus nephritis, a significant proportion of patients show persistent proteinuria after resolution of the acute nephritic process, and develop progressive renal failure. There is preliminary evidence that calcitriol and other vitamin D analogs can reduce proteinuria in patients with chronic kidney diseases. The investigators plan to conduct a randomized control study to evaluate the safety and efficacy of calcitriol in the treatment of SLE patients with persistent proteinuria. Sixty patients with clinically quiescent SLE and persistent proteinuria despite conventional therapy will be recruited. They will be treated with calcitriol for 48 weeks. Proteinuria, renal function, lupus disease activity, serum and urinary inflammatory markers will be monitored. This study will explore the potential anti-proteinuric and immunomodulating effects of calcitriol in the treatment of SLE, which is a common and life threatening disease in young adults.

NCT ID: NCT00507494 Completed - Diabetes Mellitus Clinical Trials

Influence of Pioglitazone for Renal Transplant Function in Diabetics

Start date: July 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test whether pioglitazone is able to prevent the progression of diabetic nephropathy in kidney transplant recipients with diabetes mellitus.