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Clinical Research for the Effect of Chinese and Western Medicine on Treating Rheumatoid Arthritis

Comparative Study on the Influences of Gut Microbiota of Chinese and Western Medicine for Treatment of Rheumatoid Arthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15007368
Enrollment
Unknown
Registered
2015-11-09
Start date
2015-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Rheumatoid Arthritis

Interventions

1:HuaYuTongBiFang
2:HuaYuTongBiFang+MTX
3:ZhengQingFengTongNing Pills+MTX
4:Methotrexate

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patient must be between 18 and 65 years of age; 2. The patient must meet 2010 American College of Rheumatology /The European League Against Rheumatism classification criteria for the diagnosis of active rheumatoid arthritis and Traditional Chinese Medicine for the diagnosis of "Wang Bi"; 3. Patient has discontinued all disallowed concomitant medications foe the required time prior to the first dose of study drug; 4. Patient has signed the informed consent; 5. The patients must meet Class I-III of the Xray development in RA.

Exclusion criteria

Exclusion criteria: 1. Infection, pregnancy, lactating, traumatic or other stress state; 2. Severe, progressive or uncontrolled cardiac, hepatic, renal, mental disease; 3. Severe hematologic disease including leukemia, aplastic anemia, myelodysplastic syndrome and so on; 4. Be allergic to the medicine we use in the research; 5. Use antibiotics within 1 month; 6. Patients in the Class? of RA; 7. History of other rheumatic autoimmune disease; 8. Patients with active gastrointestinal disease or pitents with peptic ulcer 4 or less weekly; 9. Patients who have previously participated in any clinical study.

Design outcomes

Primary

MeasureTime frame
ACR20/50/70;DAS28 ESR/CRP;TCM sympotoms rating scale;Metagenomic Linkage Group analysis;

Secondary

MeasureTime frame
HAQ-DI;CDAI;SDAI;Sharp's ??;TCM constitution score;

Countries

China

Contacts

Public ContactJun Wang
yuanyuanru1@genomics.cn+86 13510220140

Outcome results

None listed

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