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A Prospective cohort study of the effects of disease modifying anti- rheumatic drug on bone metabolism in Chinese patients with psoriatic arthritis

A Prospective cohort study of the effects of disease modifying anti- rheumatic drug on bone metabolism in Chinese patients with psoriatic arthritis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080436
Enrollment
Unknown
Registered
2024-01-29
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

psoriatic arthritis

Interventions

1:Methotrexate 7.5mg-15mg qw po
2:secukinumab 150mg subcutaneously at weeks 0, 1, 2, 3, and 4 and every 4 weeks thereafter

Sponsors

Peking Union Medical Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Complies with the 2006 CASPAR PsA classification standard; Plan to continue using UPA or MTX treatment for at least 3 months in the future; • Have not used any DMARDs medication before screening; • Stop csDMARDs and traditional Chinese patent medicines and simple preparations 4 weeks before screening, and stop bDMARDs 12 weeks before screening • If subjects take Nonsteroidal anti-inflammatory drug and/or glucocorticoids orally, the NSAIDs dosage must be stable at least 2 weeks before screening • Disease is active (DAPSA>14 points) Sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1)Complicated with other inflammatory arthritis or systemic autoimmune diseases (such as rheumatoid arthritis, systemic lupus erythematosus, etc.); 2)Allergies to the intended drug (UPA or MTX); 3)Pregnant or expectant women; 4)Complicated with active infections or malignant tumors; 5)Anti-osteoporosis drugs are being used (bisphosphonate, dinomimab, romozumab, Teriparatide, Calcitonin); 6)Primary osteoporosis before diagnosis of PsA; 7)Other situations where the researcher deems it inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
bone erosion ;

Secondary

MeasureTime frame
volumetric bone density ;

Countries

China

Contacts

Public ContactLin Qiao

Peking Union Medical Hospital, Chinese Academy of Medical Sciences

qiaolinmail@foxmail.com+86 138 1061 0502

Outcome results

None listed

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