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Post-marketing reevaluation of Zhuifeng Tougu capsule in treating Rheumatoid Arthritis

Post-marketing reevaluation of Zhuifeng Tougu capsule in treating Rheumatoid Arthritis

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2000002895
Enrollment
Unknown
Registered
2020-01-04
Start date
2020-01-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Rheumatoid Arthritis

Interventions

Sponsors

Temporarily not sure
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 75 years old; (2) Meet the diagnostic criteria of Rheumatoid Arthritis.

Exclusion criteria

Exclusion criteria: (1) the overlapping other rheumatism, such as systemic lupus erythematosus (sle) and sjogren's syndrome, severe patients with knee osteoarthritis, etc; (2) patients with bleeding tendency, gastrointestinal bleeding or other chronic hemorrhagic diseases within the past month; (3) women who are pregnant or breast-feeding; (4) allergic constitution or known components of the drug; (5) patients with serious diseases of heart, lung, liver, kidney, hematopoietic system, immune system, etc.

Design outcomes

Primary

MeasureTime frame
Related symptoms and signs;

Secondary

MeasureTime frame
HAQ scores;Blood sedimentation rate (ESR), rheumatoid factor (RF), and c-reactive protein (CRP) were examined;T lymphocyte subsets (CD3+, CD4+, CD8+, CD4+/CD8+);Observation on signs and symptoms of rheumatoid arthritis;VAS quantized integral;

Countries

China

Contacts

Public ContactHe Yanlin

Hinye Pharmaceutical Co., Ltd

767567825@qq.com+86 15084974669

Outcome results

None listed

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