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A observational study for iguratimod combined with methotrexate in remission or reversion bone erosion of rheumatoid arthritis

A observational study for iguratimod combined with methotrexate in remission or reversion bone erosion of rheumatoid arthritis

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021686
Enrollment
Unknown
Registered
2019-03-05
Start date
2019-03-15
Completion date
Unknown
Last updated
2019-03-18

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

Conditions

Rheumatoid arthritis

Interventions

Case Series:IGU combined with MTX

Sponsors

Nanjing Drum Tower Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 70 years, male or female; (2) Conform to 2010 ACR/EULAR RA Classification Standard (or 1987 ACR Standard) and over 6-month disease course; (3) The score of DAS 28 is over(including) 3.2; (4) Bone destruction can be seen in MRIX-ray or Color Doppler ultrasound of double hand; (5) Receive the treatment of IGU combined with MTX; (6) For those receiving NSAIDs or glucocorticoid treatment, their dose should remain unchanged for more than 2 weeks.

Exclusion criteria

Exclusion criteria: (1) Refuse to sign informed consent to participate in this trial; (2) With other serious disease requiring active treatment (cardiovascular diseases, respiratory diseases, endocrine diseases, digestive system diseases, nervous system diseases. hematological system diseases, mental illness and so on); (3) With other autoimmune diseases such as systemic lupus erythematosus, sjogren's syndrome and autoimmune liver disease; with other arthritis such as ankylosing spondylitis, psoriatic arthritis and gout. (4) With malignant tumor; (5) Be pregnancy or lactation; (6) With fatal complications such as severe infection; (7) Receive biologic DMARDs treatment; (8) Participate in other trials, and researchers think it may interfere this trail.

Design outcomes

Primary

MeasureTime frame
Joint evaluation;

Secondary

MeasureTime frame
MRI of double hand;X-ray of double hand;Pain assessment;Quality of Life Assessment;

Countries

China

Contacts

Public ContactXuebing Feng

Nanjing Drum Tower Hospital

xb.feng@163.com+86 025 83106666

Outcome results

None listed

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