Skip to content

Evaluation of the effects of JAK inhibitors on skin and lung lesions in patients with systemic sclerosis: a single center, open clinical trial

Evaluation of the effects of JAK inhibitors on skin and lung lesions in patients with systemic sclerosis: a single center, open clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030995
Enrollment
Unknown
Registered
2020-03-20
Start date
2020-03-12
Completion date
Unknown
Last updated
2020-03-30

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

Conditions

Systemic sclerosis

Interventions

single arm:JAK inhibitors

Sponsors

Dermatology Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as SSC according to the latest ACR / EULAR classification diagnostic criteria; 2. Aged >= 18 years; 3. Patients with onset of systemic sclerosis (defined as the first non Renault symptom) = 50%; (Note: before participating in the drug treatment, those who take no more than 10 mg prednisone or stable dose of mycophenolate mofetil or methotrexate for at least 6 months SSc and meet the above conditions in 1.2.3.4 shall be included in the study group; the patients in the study group are allowed to combine with other drugs at the same time, such as drugs for improving blood circulation.)

Exclusion criteria

Exclusion criteria: 1. Patients with other connective tissue diseases; 2. Patients with infection; 3. Pregnancy or preparation; 4. Patients with chronic liver disease or liver transaminase level exceeding the upper limit of normal range by 1.5 times or more; 5) Patients with forced expiratory volume / forced vital capacity = 160 mmHg and / or diastolic blood pressure > 100 mmHg) during treatment; 10. With severe cardiovascular disease (history of myocardial infarction or unstable angina within 6 months before screening, and history of thrombotic events (including stroke and transient ischemic attack) within 12 months before screening); 11. Patients treated with mycophenolate mofetil or methotrexate in an unstable background; 12. With a history of or potential for malignancy; 13. Patients with psychosis or non cooperative treatment.

Design outcomes

Primary

MeasureTime frame
Skin sclerosis;pulmonary fibrosis;

Countries

China

Contacts

Public ContactYunsheng Liang

Dermatology Hospital of Southern Medical University

yunshengliang@sohu.com+86 15973189908

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026