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A randomized, double-blind, placebo-controlled, multicenter clinical trial of Yinxieping tablets in the treatment of mild to moderate psoriasis vulgaris

A randomized, double-blind, placebo-controlled, multicenter clinical trial of Yinxieping tablets in the treatment of mild to moderate psoriasis vulgaris

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049233
Enrollment
Unknown
Registered
2021-07-27
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Psoriasis vulgaris

Interventions

Sponsors

Shaanxi Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of Western medicine for guttate or plaque psoriasis and the diagnostic criteria for TCM syndromes of psoriasis; 2. Skin lesions involving <=10% BSA; 3. PASI score<=12; 4. Aged 18-65 years, gender is not limited; 5. Those who agree to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those with other active skin diseases that may affect the assessment of the condition; 2. Have systematically received treatment with investigational drugs, biological agents and immunosuppressive agents within 1 month; 3. Received topical corticosteroids, phototherapy and other treatments within 2 weeks; 4. In a state of severe and uncontrollable local or systemic acute or chronic infection; 5. Patients with severe systemic diseases; or patients whose clinical test indicators belong to one of the following conditions: increased alanine aminotransferase or aspartate aminotransferase > 1.5 times the upper limit of normal; increased creatinine > the upper limit of normal; any one of the main indicators of blood routine (white blood cell count, hemoglobin concentration, platelet count) > the upper limit of normal value; or other abnormal laboratory examinations in patients who are not suitable for participating in this trial; 6. Patients with a history of malignant tumors and patients with primary or secondary immunodeficiency and hypersensitivity; 7. Have undergone major surgery within 8 weeks or will require such surgery during the study; 8. Pregnant or lactating patients; 9. Those with a history of alcohol, drug or drug abuse; 10. Those with a history of serious mental illness or family history; 11. Participate in other clinical trials; 12. For other reasons, the researcher believes that it is not suitable to participate in this researcher.

Design outcomes

Primary

MeasureTime frame
psoriasis area and severity index;

Secondary

MeasureTime frame
body surface area;visual analogue scale;dermatology life quality index;recurrence rate;onset time;

Countries

China

Contacts

Public ContactZhao Yiding

Shaanxi Traditional Chinese Medicine Hospital

zhaoyiding2083@126.com+86 29 87251604

Outcome results

None listed

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