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Analysis of chief physician Yan Yuhong's core prescription for psoriasis and its clinical efficacy based on data mining technology

Analysis of chief physician Yan Yuhong's core prescription for psoriasis and its clinical efficacy based on data mining technology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001404
Enrollment
Unknown
Registered
2025-07-15
Start date
2025-07-16
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

psoriasis

Interventions

1:External use of 10% urea ointment with oral Chinese herbal decoction

Sponsors

Guangdong Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age range: 18 - 70 years old gender not restricted; (2) Meets the diagnostic criteria for psoriasis vulgaris; (3) The severity of skin lesions is moderate (PASI < 10); (4) Has signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Reverse type joint type pustular type erythrodermic type psoriasis. (2) Pregnant or lactating women or those planning to get pregnant within one year. (3) Patients with severe primary diseases in the respiratory system circulatory system digestive system endocrine system and urinary system that cannot be controlled by conventional medication; patients with severe infections hepatitis tuberculosis lymphocyte proliferation hematological system abnormalities tumors; patients with severe water electrolyte and acid-base balance disorders; patients with primary or secondary immune deficiencies and hypersensitivity; or patients whose clinical test indicators fall into one of the following situations: alanine aminotransferase or aspartate aminotransferase is more than 1.5 times the upper limit of the normal value; creatinine is more than 1.5 times the upper limit of the normal value; hemoglobin is more than 20g/L above the upper limit of the normal value; platelet count is less than 75×10*9/L; white blood cell count is less than 3.0×10*9/L; blood potassium is higher than 5.5mmol/L or lower than 3mmol/L; or other laboratory test abnormalities. Researchers determine that they are not suitable to participate in this trial. (4) Patients who are known to be allergic to the drugs used in this study or allergic to the components of related drugs. (5) Patients who are currently participating in other drug clinical trials or have participated in other clinical trials within one month. (6) Patients considered not suitable for inclusion by the researchers.

Design outcomes

Primary

MeasureTime frame
Improvement rate of Psoriasis Area and Severity Index;

Secondary

MeasureTime frame
Skindex-16 Quality of Life Measure;Static Physician's Global Assessment score for psoriasis severity;Visual Analog Scale (VAS) score;Body Surface Area;Dermatology Life Quality Index (DLQI) score;

Countries

China

Contacts

Public ContactXu Haowei;Yan Yuhong

Guangdong Provincial Hospital of Traditional Chinese Medicine

2066396841@qq.com13392226818;15920395608

Outcome results

None listed

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