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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04613219
Other study ID # TY017AN
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date April 30, 2023

Study information

Verified date September 2020
Source Qianfoshan Hospital
Contact Yanfeng Hou
Phone +8615168888165
Email yfhou1016@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Acute respiratory distress syndrome (ARDS) occurs in Clinically Amyopathic Dermatomyisitis(CADM) combined with Rapidly Progressive Interstitial Lung Disease(RPILD) within 1-3 months, which leads to death of patients and is difficult to treat. Even if high doses of glucocorticoids are ineffective, there is no recommended treatment for such patients, which is a huge medical challenge.Lymphopenia is an independent risk factor for death in CADM-RPILD, but the cause of lymphopenia is unclear.In this study, the level of lymphocyte subsets in peripheral blood was detected by flow cytometer, in order to further clarify the pathogenesis of the disease, to facilitate clinical guidance of treatment, and to improve the survival rate of patients.In addition, studies have shown that INF-α levels are significantly increased in CADM patients combined with RPILD and are a poor prognostic factor for CADM-RPILD, suggesting that the interferon system plays a role in the pathogenesis of CADM and can be used as an evaluation index of the severity of CADM-RPILD.In this study, the levels of relevant cytokines including INF and IL-2, IL-17, IL-18, IL-6 were detected simultaneously, and the relationship between disease activity and lymphocyte subsets was analyzed, and the changes of lymphocyte subsets after Tofacitinib treatment were determined in order to facilitate clinical guidance of treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date April 30, 2023
Est. primary completion date April 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Age=18 years old,=80years old,no gender limit; 2. CADM of diagnosis according to Sontheimer diagnostic criteria; 3. combined with Rapidly Progressive Interstitial Lung Disease Exclusion Criteria: 1. Age<18years old,>80years old; 2. potential malignant tumor

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tofacitinib 5 MG [Xeljanz]
Treatment with Tofacitinib

Locations

Country Name City State
China Qianfoshan Hospital Jinan Shandong

Sponsors (1)

Lead Sponsor Collaborator
Jing Liang

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The level of a lymphocyte in a lymphocyte subset correlates with disease activity. 3 month