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Randomized controlled trial of powder in the treatment of rheumatoid arthritis with dampness resistance syndrome of spleen deficiency

Randomized controlled trial of powder in the treatment of rheumatoid arthritis with dampness resistance syndrome of spleen deficiency

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2100005366
Enrollment
Unknown
Registered
2021-12-02
Start date
2021-11-29
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

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1) Subjects should meet the following diagnostic criteria: ? Western diagnostic criteria: the 2010 ACR/EULAR RA classification criteria were used for comprehensive judgment; ? The standard of TCM syndrome diagnosis should refer to the Standard of RHEUMAToid Arthritis syndrome Diagnosis of spleen deficiency and Dampness resistance issued by China Association of Traditional Chinese Medicine in 2021 (T/CACM1347-2021); (2) Patients with low disease activity according to DAS28-CRP score (2.6=DAS28-CRP=3.2); (3) Aged between 18 and 70; (4) Have not been treated with palliative antirheumatic drugs (DMARDs), or have been treated with DMARD drugs in the past, but have not used such drugs for at least one month; (5) Written informed consent signed by the subject or his/her family (guardian) agreeing to participate in the study.

Exclusion criteria

Exclusion criteria: (1) history of other autoimmune diseases, such as sjogren's syndrome, systemic lupus erythematosus, etc.; Having an acute or chronic infectious disease, including hepatitis B or C infection; A previous history of cancer; Evidence of active, latent or inadequately treated Mycobacterium tuberculosis infection; (2) patients with serious cardiovascular, brain, lung, liver, kidney and hematopoietic diseases; (3) pregnant or lactating women or patients with known mental disorders; (4) Patients with hemoglobin level less than 90 g/L, white blood cell count less than 3.0×109 /L, or platelet count less than 100×109 /L; (5) patients with glomerular filtration rate below 40ml/min; (6) the level of aspartate aminotransferase or alanine aminotransferase was 1.5 times higher than the upper limit of normal range; (7) Patients with active gastroduodenal ulcer or gastritis caused by long-term use of NSAIDS; (8) Patients allergic to the test drug; (9) Screening of patients participating in other clinical trials within 4 weeks.

Design outcomes

Primary

MeasureTime frame
DAS28-CRP;

Secondary

MeasureTime frame
quality of life score;medication safety;RF;ESR;Joint symptoms and signs;CCP;ACR20;9/5000 X-ray examination of the involved joint;CRP;

Countries

China

Contacts

Public ContactHuang Runyue
ryhuang@gzucm.edu.cn+86 15889932190

Outcome results

None listed

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