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A multicenter observational clinical study of the difference in efficacy of baricitinib monotherapy and combination therapy and its effect on inflammatory markers in patients with moderate-to-severe active rheumatoid arthritis

A multicenter observational clinical study of the difference in efficacy of baricitinib monotherapy and combination therapy and its effect on inflammatory markers in patients with moderate-to-severe active rheumatoid arthritis

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081010
Enrollment
Unknown
Registered
2024-02-20
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Rheumatoid arthritis

Interventions

Therapeutic effect response group/ Non responsive treatment group :None

Sponsors

The University of Hong Kong-Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.age =18 years old; 2.comply with 1987 ACR standard or 2010 ACR/EULAR RA classification standard 3. Moderate-to-severe disease activity: DAS28 or SDAI or CDAI assessed RA to achieve moderate-to-severe activity 4. combination of drugs: combined use of traditional synthetic disease-modifying antirheumatic drugs (csDMARDs), including hydroxychloroquine (HCQ), methotrexate (MTX), leflunomide (LEF), salazosulfopyridine (SSZ), Eramod (IGU), etc.

Exclusion criteria

Exclusion criteria: 1. Combined with other types of inflammatory rheumatism and musculoskeletal diseases; 2. Currently suffering from malignant tumor or infection that may affect the level of serum inflammatory factors.

Design outcomes

Primary

MeasureTime frame
DAS-28;CDAI;ACR20 response;Serum inflammatory factor levels;

Secondary

MeasureTime frame
SDAI;ACR50/70 response;Adverse event ;Serious adverse event;

Countries

China

Contacts

Public ContactJinxian Huang

The University of Hong Kong-Shenzhen Hospital

huangjx@hku-szh.org+86 183 0755 5163

Outcome results

None listed

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