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Hyperuricemia clinical trials

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NCT ID: NCT03691688 Recruiting - Clinical trials for Coronary Artery Disease

The Long Term Effect of Low Dose Aspirin on Uric Acid in Chinese Patients With Coronary Artery Disease(AURORA)

AURORA
Start date: December 1, 2018
Phase:
Study type: Observational [Patient Registry]

The deleterious effects of hyperuricemia (HUA) on cardiovascular disease (CVD) were well established. Aspirin is the most commonly prescribed antiplatelet agent for primary or secondary prophylaxis of CVD. Only a few short-term studies in the elderly suggested low-dose aspirin, e.g., 75-100 mg/day, increases serum urate by reducing urinary uric acid excretion. However, monitoring of renal function is currently not recommended. Little is known about the long-term effect of low dose aspirin on uric acid. The principal aim of this prospective cohort study therefore is to evaluate the renal effects of long-term aspirin (100 mg/d) administration in Chinese patients with coronary artery disease or other CVDs.

NCT ID: NCT03648996 Completed - Clinical trials for Diabetes Mellitus, Type 2

Sex-related Differences in Arterial Stiffness in Type 2 Diabetics: Role of Uric Acid

Start date: November 1, 2018
Phase: Phase 2
Study type: Interventional

Three separate interventions will be undertaken with the primary outcome of improving pulse wave velocity. Initially, age and BMI-matched men and post-menopausal women, all with type 2 diabetes, will be treated with allopurinol (20 men, 20 women) for 6 months, in order to reduce serum uric acid (SUA) concentrations relative to placebo (10 men, 10 women). In a second intervention, dietary fructose will be restricted for a period of 6 months in type 2 diabetes (T2D) subjects who will maintain a stable weight (20 men, 20 women). In a third intervention, dietary fructose will be restricted for a period of 6 months in type 2 diabetes (T2D) subjects who will achieve a caloric deficit and weight reduction (20 men, 20 women). At the beginning and end of each of the studies, measures of arterial stiffness will be combined with assessments of endothelial function (flow-mediated dilation and insulin stimulated leg blood flow), measurements of systemic inflammation and oxidative stress.

NCT ID: NCT03636529 Completed - Obesity Clinical Trials

Tart Cherry Juice and Markers of Inflammation, CVD, and Diabetes

Start date: June 1, 2010
Phase: N/A
Study type: Interventional

In this study, the investigators recruited at-risk individuals (n=26) who were overweight (25.0-29.9 kg/m2) and obese (> 30.0 kg/m2) and likely to exhibit one or more conditions associated with Metabolic Syndrome (MetS). In this 12-week placebo-controlled 2 x 2 crossover dietary intervention, the investigators randomized participants to consume 240 mL (8 ounces) daily of either placebo (artificial cherry-flavored, anthocyanin-free beverage) or TCJ for 4 weeks, followed by a 4-week washout period, then consumption of the alternate beverage for 4 weeks. Subsequently, the investigators determined the effect of TCJ in at-risk participants on markers of uricemia, lipidemia, glycemia, and inflammation.

NCT ID: NCT03569020 Completed - Gout Clinical Trials

The Diet Gout Trial

DIGO
Start date: August 7, 2018
Phase: N/A
Study type: Interventional

Unhealthy diet has long been associated with high uric acid levels and gout. The DASH diet may lower uric acid levels. This study will examine the effects of the DASH diet on uric acid in adults with a history of gout.

NCT ID: NCT03534037 Recruiting - Metabolic Syndrome Clinical Trials

Urate Lowering Therapies and Left Ventricular Diastolic Dysfunction

Start date: February 1, 2020
Phase: Phase 4
Study type: Interventional

Hyperuricemia is an additional risk factor for cardiovascular disease, associating with left ventricular diastolic dysfunction in individuals with metabolic syndrome. The effect of urate-lowering therapies on left ventricular diastolic dysfunction remains unclear. The study is conducted to investigate whether febuxostat or benzbromarone might improve left ventricular diastolic dysfunction in individuals with metabolic syndrome and hyperuricemia

NCT ID: NCT03495999 Terminated - Metabolic Syndrome Clinical Trials

Hyperuricemia and Left Ventricular Diastolic Function

Start date: August 1, 2017
Phase:
Study type: Observational

Metabolic syndrome and hyperuricemia were both associated with inflammation, leading to diversities of cardiovascular disease such as left ventricular diastolic dysfunction, but the relationship among these entities remained unclear. The aim of the present study focuses on the association among hyperuricemia, diastolic dysfunction and inflammatory biomarkers in apparently healthy individuals with metabolic syndrome

NCT ID: NCT03473951 Recruiting - Healthy Clinical Trials

The Relationship Among, Serum Uric Acid, Left Ventricular Hypertrophy and Metabolic Syndrome

Start date: March 26, 2018
Phase:
Study type: Observational

Hyperuricemia is associated with the prevalence of metabolic syndrome and cardiovascular risks in diverse of the population. Whether the dose-response effects on the prevalence of metabolic syndrome and cardiometabolic risks is unclear. The present study is conducted to investigate the relationship between serum uric acid and the prevalence metabolic syndrome and left ventricular hypertrophy.

NCT ID: NCT03473444 Recruiting - Hyperuricemia Clinical Trials

Prevalence of Hyperuricemia in Pakistan

Start date: March 1, 2018
Phase:
Study type: Observational

The prevalence of hyperuricemia has rarely been investigated in developing countries Hyperuricemia, or raised serum uric acid (SUA), is the condition closely associated with gout due to the deposition of monosodium urate crystals in peripheral joints and soft tissues. Hyperuricemia is associated with an increased risk for incident hypertension, independent of traditional hypertension risk factors. This risk appears more pronounced in younger individuals and women. Cross-sectional studies show an association of hyperuricemia with the presence of CKD. Insulin resistance plays a potentially key role in the causal relationship between metabolic syndrome, type 2 Diabetes and hyperuricemia. Furthermore, it is likely that hyperuricemia and insulin resistance share a bidirectional causal effect. The rationale of this study is to determine prevalence of hyperuricemia in Pakistan.

NCT ID: NCT03425708 Recruiting - Hyperuricemia Clinical Trials

Effect of Hyperuricaemia on Chronic Renal Disease

Start date: January 1, 2017
Phase: Phase 4
Study type: Interventional

To investigate the Effect of Hyperuricaemia on Chronic Renal Disease and Intervention

NCT ID: NCT03375632 Completed - Clinical trials for Hyperuricemia With or Without Gout

Study of FYU-981 in Hyperuricemic Outpatients With or Without Gout (Effect on Two Hyperuricemic Types)

Start date: January 4, 2018
Phase: Phase 1
Study type: Interventional

To investigate the pharmacodynamics and safety of FYU-981 administered orally once a day for 14 weeks, to uric acid-overproduction type or uric acid-underexcretion type of male hyperuricemic outpatients with or without gout.