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Hyperuricemia clinical trials

View clinical trials related to Hyperuricemia.

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NCT ID: NCT00995618 Completed - Gout Clinical Trials

Study of Tranilast Alone or in Combination With Febuxostat in Patients With Hyperuricemia

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

This is a randomized, double-blind, 3-period crossover phase 2 study in patients with documented hyperuricemia to evaluate the effect of tranilast on febuxostat pharmacokinetics (PK) and pharmacodynamics (PD) and to evaluate the effect of febuxostat on tranilast PK and PD as measured by reduction in serum uric acid levels.

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: NCT00664144 Terminated - Hyperuricemia Clinical Trials

Rasburicase for the Treatment/Prevention of Hyperuricemia in Adult Patients With Relapsing Aggressive Non Hodgkin's Lymphoma

GRAAL2
Start date: July 2002
Phase: Phase 2
Study type: Interventional

The primary objective was to evaluate the efficacy of rasburicase in terms of prevention and treatment of hyperuricemia related to Tumor Lysis Syndrome (TLS) in 2 populations of adult patients, previously treated or not with urate oxidase, with relapsing aggressive non-Hodgkin's lymphoma (NHL) and at risk of TLS, presenting with hyperuricemia and/or bulky disease at diagnostic of relapse. The secondary objectives were to : - evaluate the efficacy of rasburicase in terms of renal protection, - evaluate the safety of rasburicase in the two cohorts of patients, - correlate efficacy and safety results with antibodies generation/level.

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.