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Efficacy of csDMARDs combined with L-Tryptophan supplement in the treatment of rheumatoid arthritis: a randomized controlled trial

Efficacy of csDMARDs combined with L-Tryptophan supplement in the treatment of rheumatoid arthritis: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094366
Enrollment
Unknown
Registered
2024-12-20
Start date
2024-12-23
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Rheumatoid arthritis

Interventions

Case group:csDMARDs+L-Tryptophan dietary supplement

Sponsors

Dazhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. All met the diagnostic criteria for RA revised by the American College of Rheumatology in 2010; 2. RA patients aged >=18 years and =3.0; 3. Patients who have been treated with at least one type of csDMARDS (including methotrexate, hydroxychloroquine sulfate, leflunomide, iratimod, etc.) before enrollment; 4. Patients who have good compliance, signed the informed consent form, and are able to complete the trial according to the protocol.

Exclusion criteria

Exclusion criteria: 1. Patients treated with biologics; 2. Patients with malignant diseases such as peptic ulcer, blood system diseases, mental disorders and tumors; 3. Those with previous or current medical history with inflammatory joint diseases other than rheumatoid arthritis, or those with other systemic autoimmune diseases; 4. Those with a recent history of major surgery or trauma; 5. Patients with poorly controlled concomitant diseases that are considered clinically significant by the investigator to be severe; 6. Those who have poor compliance and cannot cooperate with the completion of the test; 7. Those who have a history of depressive disorders and are taking related medications.

Design outcomes

Primary

MeasureTime frame
Disease activity score (DAS28);Swollen joint count (SJC28);Tender joint counts (TJC28);Erythrocyte sedimentation rate (ESR);C-reactive protein (CRP);Rheumatoid factor (RF);

Secondary

MeasureTime frame
Visual Analog Scal Score;Health Assessment Questionnaire for the Disability Index;

Countries

China

Contacts

Public ContactFanxin Zeng

Dazhou Central Hospital

fanxinly@163.com+86 187 2097 5685

Outcome results

None listed

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