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

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02797028
Enrollment
320
Registered
2016-06-13
Start date
2015-01-31
Completion date
2017-12-31
Last updated
2016-06-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Disease

Keywords

Hyperuricemia, endothelial function, anthocyanidins

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.

Interventions

DIETARY_SUPPLEMENTAnthocyanidins capsule

Continuous intervention for 1 years, detect the indicators in the intervention of 0,6,12 months

DIETARY_SUPPLEMENTPlacebo capsule

Continuous intervention for 1 years, detect the indicators in the intervention of 0,6,12 months

DRUGAllopurinol

Continuous intervention for 1 years, detect the indicators in the intervention of 0,6,12 months

Sponsors

Sun Yat-sen University
CollaboratorOTHER
Guangzhou General Hospital of Guangzhou Military Command
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Measurement of serum uric acid levels in all patientsup to 1 monthsSerum uric acid (mg/dl) is determined by Uric Acid kit on an automated system.

Secondary

MeasureTime frameDescription
Measurement of advanced glycation end products and its receptor level in all patientsup to 2 monthsAdvanced glycation end products and its receptor level are determined by high efficiency liquid chromatography.

Countries

China

Contacts

Primary ContactHui Dai
daihui66@sina.com020-36653321
Backup ContactYuan Zhang
1035834805@qq.com020-61653566

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026