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Hyperuricemia clinical trials

View clinical trials related to Hyperuricemia.

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NCT ID: NCT05504083 Recruiting - Hyperuricemia Clinical Trials

Evaluate the Efficacy and Safety of D-0120 in Primary Hyperuricemia Patients

Start date: September 28, 2022
Phase: Phase 2
Study type: Interventional

This is a randomized, open-label, parallel-controlled, multicenter clinical trial in primary hyperuricemia patients with or without gout.

NCT ID: NCT05476627 Recruiting - Obesity Clinical Trials

Risk Factors and Multiomics Study of Chronic Kidney Disease Caused by Metabolic Diseases

Start date: July 1, 2022
Phase:
Study type: Observational

With the development of China's economy, people's living standard have improved, and the dietary structure have changed. Metabolic diseases, such as hypertension, diabetes, hyperuricemia and obesity have gradually become an important health burden in China. The pathophysiological mechanism of renal injury caused by metabolic diseases has always been a hotspot of research. Currently, it is believed that various mechanisms including the activation of Renin-Angiotensin-Aldosterone System, vascular endothelial dysfunction, oxidative stress and inflammatory process may be involved. Although there are differences in renal pathological manifestations caused by different metabolic diseases, the kidney will eventually present ischemic changes and fibrosis with the progression of the disease. So there must be some common pathogenesis. This study is designed to build a disease cohort of patients with chronic kidney disease caused by metabolic diseases, to identify risk factors leading to disease progression and to explore biomarkers for early diagnosis and treatment of kidney damage.

NCT ID: NCT05434858 Recruiting - Hyperuricemia Clinical Trials

Imagery as Biomarker of Gout

TIGER
Start date: September 9, 2022
Phase: N/A
Study type: Interventional

The objective of this study is to determine whether MSU crystal deposits visualized on ultrasound and/or DECT are associated with the development of symptomatic gout (according to ACR 2015 / EULAR criteria) over 5 years in hyperuricemic individuals.

NCT ID: NCT05406830 Recruiting - Clinical trials for Asymptomatic Hyperuricemia

Efficacy Study of Acupuncture on Asymptomatic Hyperuricemia

Start date: July 13, 2022
Phase: N/A
Study type: Interventional

hyperuricemia (HUA) is an important risk factor for various chronic diseases, such as gout, and the current treatment programs for HUA are not ideal. It is urgent to find new methods to prevent and treat HUA and to carry out early clinical intervention. Acupuncture is commonly used for the treatment of HUA, while the evidence for its efficacy is still uncertain. This clinical trial aimed to evaluate the efficacy and safety of manual acupuncture for asymptomatic HUA.

NCT ID: NCT05385003 Recruiting - Clinical trials for Subjects With Hyperuricemia

Effect of Prebiotics on Hyperuricemia

Start date: May 14, 2022
Phase: N/A
Study type: Interventional

Hyperuricemia is a major risk factor for many chronic diseases. Recently, dysbiosis of gut microbiota has been reported to play an important role in the pathogenesis of Hyperuricemia. Animal studies have demonstrated that administration of prebiotics help delay the progression of Hyperuricemia through several mechanisms. This trial aims to examine its protective effect in humans.

NCT ID: NCT05342285 Recruiting - Clinical trials for Cardiovascular Diseases

Flow Mediated Dilation in Association With Hyperuricemia

Start date: July 30, 2022
Phase:
Study type: Observational

Assess cardiovascular affection and subclinical atherosclerosis in patients with systemic lupus using the non invasive flow mediated dilation. evaluate the role of uric acid as independent marker of cardiovascular risk in systemic lupus patient

NCT ID: NCT05226013 Recruiting - Hyperuricemia Clinical Trials

Tolerance, Pharmacokinetics / Pharmacodynamics (PK / PD) and Immunogenicity of Pegylated Uric Acid Oxidase for Injection in Healthy Adults and Hyperuricemia Volunteers

Start date: December 8, 2021
Phase: Phase 1
Study type: Interventional

A randomized, double-blind, placebo-controlled study of tolerance, pharmacokinetic / pharmacodynamics (PK / PD) and immunogenicity of single administration of PEG uric oxidase for injection in healthy adults and hyperuricemia volunteers.

NCT ID: NCT04953533 Recruiting - Gout Clinical Trials

Research and Development of a New Technology for Detection of Abnormal Excretion of Intestinal Uric Acid Involved in the Incidence of Gout

Start date: July 6, 2021
Phase:
Study type: Observational

To evaluate differences in specific SNPs and intestinal microflora between patients with gout and hyperuricemia and healthy controls.

NCT ID: NCT04801745 Recruiting - Diet, Healthy Clinical Trials

Vegan Diet, Amla Fruits and Uric Acid

Start date: March 20, 2021
Phase: N/A
Study type: Interventional

This is an intervention study aiming to test the effectiveness of a vegan diet, My Plate with low purine choices, and amla fruits on uric acid and other cardiometabolic risk factors in individuals with high serum uric acid levels.

NCT ID: NCT04733079 Recruiting - Gout Clinical Trials

Treat-to-target by Email During Urate-lowering Therapy in Gout

GOUTEmail
Start date: December 15, 2021
Phase: N/A
Study type: Interventional

Gout is secondary to urate crystal deposition after chronic elevation of serum urate level (SUL). Long-term lowering SUL below 360 µmol/L allows dissolution of deposited crystals and disease cure. There is currently a paradoxical observation: while urate-lowering therapy (ULT) is available and efficient there is an increase of gout prevalence and severity. The apparent failure of ULT in gout management is due to several causes including unadjusted dosage, no SUL verification, irregular follow-up and low treatment compliance. In contrast, a nurse-led treat-to-target (T2T) strategy with regular adaptations of ULT until reaching SUL target allows gout cure in more than 90% of patients. We hypothesize that an electronic messaging-led T2T strategy will allow obtaining similar results. The aim of this study is to demonstrate that email-led T2T strategy during ULT is superior to usual care.