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A Multi-Center Evidence-Based Evaluation Study of Key Traditional Chinese Medicine Staging and Treatment Techniques and Strategies for Rheumatoid Arthritis

A Multi-Center Evidence-Based Evaluation Study of Key Traditional Chinese Medicine Staging and Treatment Techniques and Strategies for Rheumatoid Arthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077155
Enrollment
Unknown
Registered
2023-10-31
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-11-06

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

Conditions

rheumatoid arthritis

Interventions

WM group early stage :NA
TCM group early stage :NA
Subacute Stage RA WM Group:NA
Subacute Stage RA TCM Group:NA
Chronic Stage RA WM Group:NA
Chronic Stage RA TCM Group:NA

Sponsors

Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ?Patients who meet the 2010 ACR/EULAR classification criteria for Rheumatoid Arthritis (RA). ?Patients in the early stage, subacute stage, or chronic stage of RA (Rheumatoid Arthritis), specifically: Early-stage or subacute-stage RA patients. Chronic-stage RA patients (Late-stage Rheumatoid Arthritis). ?DAS28 (Disease Activity Score in 28 joints) > 2.6. ?Patients with RA who meet one of the following TCM syndrome patterns: Spleen deficiency with wind-cold-dampness obstruction syndrome. Spleen deficiency with damp-heat-stasis obstruction syndrome. Spleen-kidney deficiency with phlegm-stasis obstruction syndrome. ?Age between 18 and 65 years old. ?Patients who are informed about the study and provide their voluntary consent to participate.

Exclusion criteria

Exclusion criteria: ?Patients with severe organ damage or those suffering from severe mental disorders. ?Patients who have allergies to the drugs involved in the research protocol or have contraindications for their use.

Design outcomes

Primary

MeasureTime frame
ACR20/50/70 Improvement Rate;DAS28 Remission Rate;DAS28 Low Activity Rate;

Secondary

MeasureTime frame
CDAI Remission Rate;SDAI Remission Rate;Incidence Rate of Adverse Events;SF-36 Health Survey;Health Assessment Questionnaire Disability Index" (HAQ-DI);Functional Assessment of Chronic Illness Therapy - Fatigue;Traditional Chinese Medicine Syndrome Score;

Countries

China

Contacts

Public ContactChengping Wen

Zhejiang Chinese Medical University

wengcp@163.com+86 21 8661 3644

Outcome results

None listed

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