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Strategic management of anti-rheumatoid arthritis treatment.

Strategic management of anti-rheumatoid arthritis treatment.a random, open clinical trial.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000469
Enrollment
Unknown
Registered
2009-07-12
Start date
2009-07-15
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

A:LEF 10mg qd + HCQ 0.2 bid.
B:LEF 10mg qd

Sponsors

Peking University People's hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 to 65 years old; 2. RA patients with active disease;1) Diagnosed based on the 1987 revised American College of Rheumatology (ACR) criteria for RA: (1) Morning stiffness>=1h; (2) Arthritis of three or more joint areas, >=6 weeks; (3) Arthritis of hand joints, >=6 weeks; (4) Symmetric arthritis, >=6 weeks; (5) Rheumatoid nodules; (6) Serum rheumatoid factor; (7) Radiographic changes. Satisfied at least four of these seven criteria; 2. The DAS28 score more than 5.1 is defined as active disease; 3. To be able to and willing to provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergy to leflunomide(LEF),methotrexate(MTX) and hydroxychloroquine(HCQ); 2. Stage IV of joints according to the American College of Rheumatology(ACR); 3. Body Weight =10mg/d within 1 month before enrolment.

Design outcomes

Primary

MeasureTime frame
The efficiency and recurrence rate;

Secondary

MeasureTime frame
Lab test;Clinical symptoms and signs;Sharp score;The doctor's and the patient's self assessmen;

Countries

China

Contacts

Public ContactZhanguo Li
zgli98@yahoo.com+86 010 88324172

Outcome results

None listed

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