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Randomized controlled study on the treatment of gouty arthritis (damp-heat accumulation syndrome) with Jinju Qubing formula

Clinical evaluation of Jinju Qubi formula

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002502
Enrollment
Unknown
Registered
2025-12-24
Start date
2023-10-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

gouty arthritis

Interventions

experimental group :jinjuqubifang
control group:Fesibut tablets

Sponsors

Affiliated Hospital of Gansu University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Voluntary enrollment with signed informed consent; 2) Compliance with the 2015 American College of Rheumatology/European League Against Rheumatism Gout Classification Criteria; 3) Age 18-60 years (gender unrestricted), with self-care capacity; 4) Patients demonstrating treatment adherence, completion of scheduled regimens, and cooperation with clinical observers for follow-up monitoring; 5) Participants fully comprehend the study's objectives, their condition specifics, trial medication characteristics, treatment protocols, and potential risks before signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Patients with comorbidities causing concurrent joint pain; 2) Those with severe primary diseases (hematopoietic system disorders, liver/kidney diseases, pulmonary conditions) or psychiatric disorders; 3) Pregnant or breastfeeding women; 4) Participants currently enrolled in other drug-related clinical trials or research programs; 5) Individuals exhibiting mental, cognitive, or consciousness abnormalities that impair treatment compliance; 6) Suspected secondary HUA cases (e.g., those undergoing tumor radiotherapy/chemotherapy, anti-tuberculosis medication use); 7) Subjects deemed unsuitable by investigators due to frequent job relocations, unstable living environments, or other factors likely causing follow-up discontinuation; 8) Patients with severe hypertension or cardiovascular/cerebrovascular diseases; 9) Those allergic to traditional Chinese medicine or febuxostat.

Design outcomes

Primary

MeasureTime frame
Uric acid;erythrocyte sedimentation rate (ESR) ;C reactive protein ;

Secondary

MeasureTime frame
Visual Analogue Scale for Pain;Traditional Chinese Medicine Syndrome Rating;

Countries

the People's Republic of China (PRC)

Contacts

Public ContactXie Xingwen

Affiliated Hospital of Gansu University of Chinese Medicine

1522874679@qq.com15002591615

Outcome results

None listed

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