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The Construction and Implementation of Traditional Chinese Medicine Clinical Pathway Program for Acute Gout

The Construction and Implementation of Traditional Chinese Medicine Clinical Pathway Program for Acute Gout

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000660
Enrollment
Unknown
Registered
2025-04-06
Start date
2025-04-10
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Gout

Interventions

TCM Clinical Pathway Group:Comprehensive TCM Treatment
Not TCM Clinical Pathway Group: Non-traditional Chinese medicine clinical pathway treatment: colchicine and/or nonsteroidal anti-inflammatory drugs (NSAIDs) and/or corticosteroids etc.

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria are as follows: 1)Meet the Western medicine diagnostic criteria for gout; 2)Have a VAS score of 3=VAS<7 with the duration from gout onset to enrollment =1 week; 3)Meet the TCM diagnostic criteria for dampness-heat stagnation syndrome; 4)Be aged between 18 and 70; 5)Voluntarily participate in the study and sign the consent form.

Exclusion criteria

Exclusion criteria: The exclusion criteria are as follows: 1)Patients with secondary gout; 2)Those who have taken oral contraceptives or undergone hormone replacement therapy (with a prednisone dosage >10mg/d) within 3 months before the trial; 3)Patients with severe gastrointestinal diseases or ulcers; 4)Patients with severe dysfunction of important organs (heart brain liver kidney etc.) or malignant tumors; 5)Patients with mental illnesses long-term alcohol/drug abuse; 6)Pregnant or breastfeeding women; 7)Individuals with allergic constitutions or known allergies to components of the study drugs; 8)Those participating in other clinical trials that may affect the evaluation of this study.

Design outcomes

Primary

MeasureTime frame
visual analogue scale;

Secondary

MeasureTime frame
Inflammatory markers:ESR CRP;Serum uric acid;

Countries

China

Contacts

Public ContactSunlu

Guangdong Provincial Hospital of Chinese Medicine

sunlu@gzucm.edu.cn+86 138 2605 5952

Outcome results

None listed

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