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Cost-effectiveness of adalimumab "reduction strategies" in the treatment of rheumatoid arthritis: a multicenter, prospective, real-world observational study

Cost-effectiveness of adalimumab "reduction strategies" in the treatment of rheumatoid arthritis: a multicenter, prospective, real-world observational study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300072896
Enrollment
Unknown
Registered
2023-06-27
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

rheumatoid arthritis

Interventions

Adalimumab full dose group (Adalimumab, 40mg/2 weeks, subcutaneous injection):None
Adalimumab tapering group (Adalimumab tapering combined with methotrexate therapy. The recommended dosage of adalimumab is as follows: Adalimumab, 40mg/2 weeks, subcutaneous injection, reduce the dose
"Triple therapy" group (triple therapy is applied. According to the patient's condition and willingness of patients, three traditional synthetic anti-rheumatic drug combination treatment could be appl
Leflunomide, 10-20mg once daily
Sulfasalazine, orally, 500mg-1000mg each time, 3-4 times a day
Hydroxychloroquine, orally, 0.2g to 0.4g, once a day.):None

Sponsors

School of clinical medicine & the first affiliated hospital of chengdu Medical college
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) voluntary informed consent; (2) Meet the RA classification standard of ACR 1987 or the RA classification standard of ACR/EULAR 2010; (3) Current initiation or preparation of adalimumab or "triple therapy" as assessed by the clinician.

Exclusion criteria

Exclusion criteria: (1) in the systemic acute or chronic infection period, or have a history of active tuberculosis; (2) malignant tumor subjects; (3) Moderate to severe heart failure (New York Heart Society grades 3-4); (4) Pregnant and lactating women; (5) Allergic to the ingredients of the study drug.

Design outcomes

Primary

MeasureTime frame
DAS28 score;Total cost;HAQ score;

Countries

China

Contacts

Public ContactDang Wantai

School of clinical medicine & the first affiliated hospital of chengdu Medical college

694466576@qq.com+86 185 3873 7790

Outcome results

None listed

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