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Clinical study of the efficacy of baricitinib for refractory adult-onset Still's disease.

Clinical study of the efficacy of baricitinib for refractory adult-onset Still's disease.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200061599
Enrollment
Unknown
Registered
2022-06-29
Start date
2020-08-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Adult-onset Still's disease

Interventions

Group 1:Baricitinib therapy

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who fulfill Yamaguchi's diagnostic criteria after evaluation; 2. Patients with a clear diagnosis of AOSD after the possibility of infection, malignancy, and other rheumatic immune diseases have been excluded; 3. Patients with refractory AOSD for whom conventional treatment is ineffective or ineffective, further leading to relapse; 4. Aged 18-65 years; 5. Voluntarily subjected to the trial and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who have been diagnosed with other rheumatic immune diseases such as systemic lupus erythematosus, dry syndrome, myositis, or dermatomyositis; 2. Those with a combination of serious primary diseases of the cardiovascular, hepatic, renal, and hematopoietic systems, psychiatric patients; 3. The presence of active infectious diseases or chronic infectious diseases; 4. Women who are pregnant, breastfeeding, or have a pregnancy planned during treatment; 5. Those with a history of drug or substance abuse or alcoholism; 6. The investigator deemed cases inappropriate for inclusion in this clinical study.

Design outcomes

Primary

MeasureTime frame
Systemic score;Pred dosage;

Countries

China

Contacts

Public ContactXin Li

Tianjin Medical University General Hospital

limbourg@163.com+86 13302123520

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026