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Expression of decorin in skin and peripheral blood affected by systemic sclerosis

Expression of decorin in skin and peripheral blood affected by systemic sclerosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104265
Enrollment
Unknown
Registered
2025-06-13
Start date
2025-06-30
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Systemic sclerosis

Interventions

Case group:None
Control group:None

Sponsors

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. SSc patient selection: (1) Patients must meet the classification criteria for systemic sclerosis established by the American College of Rheumatology (ACR) in 1980 or the American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) in 2013; (2) The age of the patient should be greater than or equal to 18 years old at the time of enrollment; 2. Selection of healthy volunteers: Healthy volunteers must be aged 18 years or older and have no history of acute or chronic infection.

Exclusion criteria

Exclusion criteria: 1. SSc patients: (1) Significant health problems or diseases, including (but not limited to) the following: poorly controlled hypertension (>=160/95 mmHg), congestive heart failure (New York Heart Association criteria class III or IV), poorly controlled diabetes mellitus or poor functional status that makes it impossible to take care of oneself, other autoimmune diseases, tumors; (2) The total number of peripheral blood leukocytes =160/95 mmHg), congestive heart failure (New York Heart Association criteria class III or IV), poorly controlled diabetes mellitus or poor functional status that makes it impossible to take care of oneself, other autoimmune diseases, tumors; (2) The total number of peripheral blood leukocytes < 3 000 /µL, or the < platelets 100 000 /µL or the neutrophil < 1 500 /µL or the hemoglobin < 85 g/L at screening; (3) Pregnant, pregnant or lactating women; (4) Current infection, chronic or recurrent infectious diseases, or evidence of latent tuberculosis infection; (5) Known infection with human immunodeficiency virus, hepatitis B virus or hepatitis C virus at the time of screening; (6) Any other conditions that the investigator considers unsuitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Decorolican;

Secondary

MeasureTime frame
Peripheral blood mononuclear cell;Cytockines;

Countries

China

Contacts

Public ContactLingli Dong

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology

tjhdongll@163.com+86 27 83665518

Outcome results

None listed

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