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Investigation of the Atherogenic Effects of Uric Acid-modified in Endothelial Dysfunction and the the Preventional Mechanism by Anthocyanidines

Phase 4
Conditions
Cardiovascular Disease
Interventions
Dietary Supplement: Anthocyanidins capsule
Dietary Supplement: Placebo capsule
Registration Number
NCT02797028
Lead Sponsor
Guangzhou General Hospital of Guangzhou Military Command
Brief Summary

The purpose of this study is to confirm the protective effect and mechanism of anthocyanins on hyperuricemia patients with Cardiovascular disease.

Detailed Description

Hyperuricemia patients who have the ability to complete the intervention study in the early stage of study were selected as the research subjects. A randomized controlled double blind control method was used to study the effect of one year of anthocyanins intervention. Serum UA levels, oxidative stress, AGEs, and endothelial function are detecting in patients with hyperuricemia who were treated with anthocyanins and placebo. Providing scientific basis of anthocyanins for the treatment with hyperuricemia and delaying atherosclerosis.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
320
Inclusion Criteria
  • Serum uric acid >420μmol/L (7mg/dL) in male, >360μmol/L (6mg/dL) in female identified as hyperuricemia patients.
Exclusion Criteria
  • Age more than 60 years and less than 30 years old;
  • acute infection, tumor, recent surgery, need for hemodialysis and autoimmune diseases.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Anthocyanidins capsuleAnthocyanidins capsuleSimple hyperuricemia patients and with coronary heart disease in hospital. Double blind, randomized method. The experimental group taking anthocyanins capsule.
Placebo capsulePlacebo capsuleSimple hyperuricemia patients and with coronary heart disease in hospital. Double blind, randomized method. Control group taking placebo capsule
AllopurinolAllopurinolThe experimental group taking allopurinol.
Primary Outcome Measures
NameTimeMethod
Measurement of serum uric acid levels in all patientsup to 1 months

Serum uric acid (mg/dl) is determined by Uric Acid kit on an automated system.

Secondary Outcome Measures
NameTimeMethod
Measurement of advanced glycation end products and its receptor level in all patientsup to 2 months

Advanced glycation end products and its receptor level are determined by high efficiency liquid chromatography.

Trial Locations

Locations (1)

General Hospital of Guangzhou Military Command of People's Liberation Army

🇨🇳

Guangzhou, Guangdong, China

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