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Effect of Gegen Qinlian Decoction on hyperuricemia

Effect of Gegen Qinlian Decoction on hyperuricemia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038257
Enrollment
Unknown
Registered
2020-09-15
Start date
2020-09-15
Completion date
Unknown
Last updated
2020-12-07

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

Conditions

Hyperuricemia

Interventions

Trial group:Drug intervention
control group:no intervention

Sponsors

Huadong Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. After stopping high purine and high protein diet for 2 weeks or antiuricemic drugs for 2 weeks, the fasting blood uric acid was measured twice on different days: 420 µ mol / L (7Mg / dl) 540 µ mol / L (9mg / dl); according to the classification and diagnostic criteria of hyperuricemia, it belongs to the type of poor uric acid excretion; 2. Male, 18-75 years old; 3. Asymptomatic hyperuricemia patients had no gout arthritis, gout stone, uric acid kidney stone and other gout clinical manifestations; 4. Patients with single TCM damp heat constitution type; 5. The subjects must voluntarily participate in the study and abide by the research regulations, understand and abide by the dosage and follow-up plan, and voluntarily sign the written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with allergic constitution or allergic to this drug, and those with weak constitution; 2. Patients with severe primary diseases such as cardiovascular, cerebrovascular, liver, kidney and hematopoietic system, and mental patients; 3. Patients with secondary hyperuricemia, such as leukemia, myeloma, renal failure, polycystic kidney disease, some endocrine diseases, some drugs such as diuretics, aspirin, antituberculosis drugs, etc; 4. Patients who fail to use drugs and complete treatment according to the regulations, unable to judge the efficacy or incomplete data, which affect the efficacy or safety judgment.

Design outcomes

Primary

MeasureTime frame
Serum uric acid;

Countries

China

Contacts

Public ContactWang Xiaojun

Huadong Hospital

13681803275@163.com+86 13681803275

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026