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The antipruritic effect of qingpeng ointment in the localized non-exudative eczema and the changes of cytokines before and after treatment.

The antipruritic effect of qingpeng ointment in the localized non-exudative eczema and the changes of cytokines before and after treatment.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016190
Enrollment
Unknown
Registered
2018-05-17
Start date
2018-05-17
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

localized eczema

Interventions

Qing peng cream group:apply Qing peng cream, bid
Qingpeng ointment base:apply Qingpeng ointment base, bid

Sponsors

Department of Dermatology, Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. aged from 18-80 years male and female; 2. Clinically Diagnosed localized chronic eczema, Skin involvement for 1% to 15% of body surface areapatients; 3. The disease has no obvious cause; 4. Participant fully understands the content of the clinical trial, is willing to attend the research voluntary andsign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. allergic to the study drugs; 2. with severe disease in the liver, kidney, and/or blood; with autoimmune diseases, chronic serious infection, diabetes, mental diseases, substance abuse, and/or alcoholic; with the malignant tumor or other serious diseases that may compromise the accuracy of efficacy evaluation for the study drug; 3. apply corticosteroids cream within 2 weeks; have taken systemic corticosteroids or other systemic immune inhibitors (e.g. Tripterygium wilfordii et al.) within 4 weeks; 4. rash on face, skin folds such as anus, vulva; 5. Skin lesions with a total area of more than 15% of the body surface area or less than 1%; 6. other reasons that researchers think that should not be selected.

Design outcomes

Primary

MeasureTime frame
VAS;EASI;Four-item itch questionnaire;

Countries

China

Contacts

Public ContactXU WEI

Department of Dermatology, Beijing Friendship Hospital, Capital Medical University

2403649155@qq.com+86 18611015100

Outcome results

None listed

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