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Evaluation of the Efficacy and Safety of Targeted Treatment-Based Biologics Maintenance Strategies in Elderly Patients with Rheumatoid Arthritis

Evaluation of the Efficacy and Safety of Targeted Treatment-Based Biologics Maintenance Strategies in Elderly Patients with Rheumatoid Arthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400092188
Enrollment
Unknown
Registered
2024-11-12
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Rheumatoid arthritis

Interventions

Clinical remission group:None
Low disease activity group:None

Sponsors

Meishan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age = 65 years; 2. Meets the 2010 American College of Rheumatology (ACR) / European League Against Rheumatism (EULAR) classification criteria for RA diagnosis; 3. Has undergone at least 3 months of treatment with one or more conventional synthetic disease-modifying antirheumatic drugs (CSDMARDS) combined with standard-dose TNF inhibitors (tumor necrosis factor inhibitors, TNFi), with an improvement in SDAI = 50% after treatment.

Exclusion criteria

Exclusion criteria: 1. Participation in other drug observer studies within the last 6 months. 2. Use of oral glucocorticoids during the screening period, or glucocorticoid injections into the joint cavity, intramuscularly, or intravenously within the past month. 3. History of active peptic ulcer disease. 4. Patients with significant hematologic disorders and abnormal lab test results (WBC < 4 × 10^9/L or PLT < 100 × 10^9/L). 5. ALT = 2 × ULN, AST = 2 × ULN, GFR = 40 ml/min. 6. History of acute or chronic infections (including, but not limited to, viral hepatitis, herpes zoster virus, tuberculosis, etc.). 7. History of malignant tumors, decompensated heart failure or severe hypertension, epilepsy, and other neurological disorders. 8. History of alcoholism within the past 2 years.

Design outcomes

Primary

MeasureTime frame
SDAI score;

Secondary

MeasureTime frame
Adverse event monitoring;

Countries

China

Contacts

Public ContactZehui Liao

Meishan People's Hospital

287250004@qq.com+86 183 2845 3515

Outcome results

None listed

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