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Hyperuricemia clinical trials

View clinical trials related to Hyperuricemia.

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NCT ID: NCT00978653 Completed - Clinical trials for Chronic Kidney Disease

The Effect of Uric Acid Decrement on Endothelial Function in Patients With Chronic Renal Failure

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

In this prospective study, the investigators aimed to evaluate the effects of improved hyperuricemia, a minor cardiovascular risk factor, on endothelial dysfunction in patients with chronic kidney disease.

NCT ID: NCT00955981 Completed - Hyperuricemia Clinical Trials

Gout Dose Response Study

Start date: July 2009
Phase: Phase 2
Study type: Interventional

To compare the proportion of subjects whose serum urate (sUA) level is < 6.0 mg/dL after 28 days of dosing by treatment group.

NCT ID: NCT00921375 Completed - Hyperuricemia Clinical Trials

Safety and Efficacy of TULY (Rasburicase) in Prevention and Treatment of Malignancy-associated Hyperuricemia

Start date: February 2010
Phase: Phase 3
Study type: Interventional

This study is a prospective, open-label, multicentre study. Hundred eligible patients with stage III or IV non-Hodgkin lymphoma (NHL) or acute lymphoblastic leukemia (ALL) with a peripheral white blood cell (WBC) count of > 25,000/µL or any leukemia or lymphoma with plasma uric acid level of at least 8 mg/dL will be treated with rasburicase 0.20 mg/kg body weight intravenously for 4 days. The primary endpoints viz., the percentage of reduction in plasma uric acid at 4 hrs after uric acid-lowering therapy, plasma uric acid AUC 0-96 hr and incidence of adverse events will be assessed during 11 days study period.

NCT ID: NCT00919243 Completed - Heart Failure Clinical Trials

Prednisone for Heart Failure Patients With Hyperuricemia

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

Hyperuricemia is a very common finding in patients with heart failure. It is usually related to diuretic use and deteriorated renal function. The recently evidence showed that uric acid (UA) lowering therapy may improve clinical status in symptomatic heart failure patients with hyperuricemia. In their clinical practice, the investigators found that glucocorticoids could dramatically lower UA while improving renal function. Thus the investigators design this randomized head to head study to test our hypothesis that prednisone have the same efficacy to allopurinol on lowering UA and could improve renal function at the same time.

NCT ID: NCT00868673 Completed - Metabolic Syndrome Clinical Trials

The Role Of Fructose and Uric Acid In the Development of Obesity and Metabolic Syndrome

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

The purpose of this study is to determine if a low fructose intake could have an impact on weight loss, uric acid levels and the components of the metabolic syndrome (glucose, cholesterol, triglycerides, insulin resistance, high blood pressure).

NCT ID: NCT00756964 Completed - Hyperuricemia Clinical Trials

Lowering Serum Uric Acid to Prevent Acute Kidney Injury

RasbAKI
Start date: October 2008
Phase: Phase 2
Study type: Interventional

Acute kidney injury is associated with a rise in serum uric acid during cardiovascular surgery and can cause poor blood flow to the kidneys making them vulnerable to kidney injury. We hypothesize that hyperuricemia, particularly if chronic and marked, is a risk factor for acute kidney injury. The preoperative lowering of serum uric acid will reduce the incidence of acute kidney injury following cardiovascular surgery.

NCT ID: NCT00741442 Completed - Hyperuricemia Clinical Trials

A Study of RDEA806 in Hyperuricemic Subjects With Symptomatic Gout

Start date: July 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether RDEA806 is effective in the treatment of hyperuricemia in gout patients.

NCT ID: NCT00631579 Completed - Lymphoma Clinical Trials

Rasburicase as a Uricolytic Therapy for Hyperuricemia in Patients With Leukemia or Lymphoma

Start date: April 2003
Phase: Phase 2
Study type: Interventional

The primary objectives of the study are to evaluate the safety and the efficacy in patients with malignant lymphoma or acute leukemia who are repeatedly administered for SR29142 5 days in two dosage groups. Secondary objectives are to determine the pharmacokinetic (PK) parameters of SR29142 , to assess anti-SR29142 antibody production in patients with malignant lymphoma and acute leukemia, and to estimate the optimal dosage of SR29142 for Japanese patients from the results of efficacy and safety evaluations.

NCT ID: NCT00563771 Completed - Hyperuricemia Clinical Trials

Rasburicase for Treatment of Hyperuricemia in Children and Adolescence Patients With Tumor Lysis Syndrome

Start date: March 2003
Phase: Phase 4
Study type: Interventional

To provide treatment opportunity to children and adolescent patients with hematologic malignancies by supplying the delayed marketed product and also to observe the efficacy and safety of rasburicase used in the treatment of hyperuricemia

NCT ID: NCT00422318 Completed - Heart Failure Clinical Trials

Treatment of Hyperuricemia in Patients With Heart Failure

Start date: January 2004
Phase: Phase 4
Study type: Interventional

The study aims to assess (I) the contribution of UA itself to the CHF pathophysiology and (II) to test the effect of lowering UA by uricosuric treatment in CHF.