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Efficacy of Modified Shenling Baizhu Powder in the Treatment of Atopic Dermatitis with Spleen Deficiency and Dampness Retention Syndrome: A Randomized, Double-Blind, Multicenter Clinical Trial

Efficacy of Modified Shenling Baizhu Powder in the Treatment of Atopic Dermatitis with Spleen Deficiency and Dampness Retention Syndrome: A Randomized, Double-Blind, Multicenter Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002193
Enrollment
Unknown
Registered
2025-11-17
Start date
2025-11-15
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Atopic Dermatitis

Interventions

Intervention:Loratadine + Vitamin E Cream + Shenling Baizhu Powder Modified Prescription
control:Loratadine + vitamin E cream + placebo

Sponsors

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Patients meeting the diagnostic standards of Western medicine; 2) Patients meeting the diagnostic standards of traditional Chinese medicine; 3) Patients with mild to moderate atopic dermatitis (SCORAD score 0-50); 4) Age 18-70 years old, regardless of gender; 5) The patient did not use other AD drugs such as antihistamines, immunosuppressants, glucocorticoids, biologics, etc. in the past 2 weeks or could affect AD phototherapy; 6) Agree to participate in the study and voluntarily sign the informed consent form and agreement.

Exclusion criteria

Exclusion criteria: 1) Those who are allergic to the study medication; 2) Patients with other serious skin diseases and heart, liver and kidney diseases (such as endocrine, cardiovascular and cerebrovascular diseases, Parkinson's disease, malignant tumors), diabetes and mental diseases; 3) Pregnant and lactating women, etc.; 4) Patients with abnormal electrocardiogram, liver and kidney function, or patients with possible itching; 5) Those who are not suitable for participating in the clinical trial after assessment by the investigator.

Design outcomes

Primary

MeasureTime frame
Scoring Atopic Dermatitis;

Secondary

MeasureTime frame
Dermatology Life Quality Index;Investigator Global Assessment;Traditional Chinese Medicine Syndrome Score Scale;inflammatory;

Countries

CHINA

Contacts

Public Contactzhaojingxia

Beijing Hospital of Traditional Chinese Medicine, Capital Medical University

zhaojingxia@bjzhongyi.com+86 135 2089 8350

Outcome results

None listed

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