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Clinical observation on reducing uric acid in treating gouty arthritis intermittent and hyperuricemia with Kang-acid tea

Clinical observation on reducing uric acid in treating gouty arthritis intermittent and hyperuricemia with Kang-acid tea

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070968
Enrollment
Unknown
Registered
2023-04-27
Start date
2023-05-01
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

gouty arthritis?hyperuricemia

Interventions

Treatment group:Basic therapy + Kang-acid tea

Sponsors

Yunnan Hospital of Traditional Chinese Medicine / The No.1 Affiliated Hospital of Yunnan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for gout of the American College of Rheumatology; 2. Meet the criteria for intermittent staging of gouty arthritis; 3. Blood uric acid value: male =420umol/L, female =360umol/L; 4. Routine findings of liver and kidney function and hematuria were normal; 5. Age between 18 and 70 years old (including 18 and 70 years old), both male and female; 6. Volunteer to participate in this study, agree to enter clinical study, and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Secondary gout, joint lesions caused by rheumatoid arthritis, suppurative arthritis, traumatic arthritis, silver shag arthritis, pseudogout, lupus erythematosus and other diseases. Chemotherapy, radiotherapy, chronic lead poisoning, acute obstructive nephropathy and other joint lesions. 2. Patients with late deformities, disabilities, loss of labor force, and cardiovascular and cerebrovascular diseases induced by pain. 3. Severe heart, brain, liver, kidney and other complications or other serious primary diseases, such as tumor or AIDS. 4. Blood Cr, ALT, AST and BUN exceed 1.5 times of the normal value. 5. Participants are participating in other drug clinical trials, or the drug clinical trial group is less than 1 week; 6. Patients who fail to complete drug treatment as prescribed by the doctor, cannot judge the efficacy, have poor compliance, or have incomplete data; 7. Allergic constitution (known allergic to the components of this medicine); 8. Pregnant or lactating women or women who intend to become pregnant; 9. History of neuropsychiatric disorders (epilepsy, depression, etc.); 10. Suspected or existing history of alcohol or drug abuse, or other medical conditions that reduce or complicate enrollment, such as frequent changes in the work environment, may cause loss of follow-up.

Design outcomes

Primary

MeasureTime frame
erythrocyte sedimentation rate, ESR;C-reactive protein, CRP;blood uric acid, BUA;urine uric acid, UUA;

Secondary

MeasureTime frame
Routine blood testing;Liver function test;

Countries

China

Contacts

Public ContactChen Yanlin

Yunnan Hospital of Traditional Chinese Medicine / The No.1 Affiliated Hospital of

ynkmpzj@126.com+86 13888340962

Outcome results

None listed

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