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Real world study of Benvitimod cream in the treatment of chronic simple lichen

Real world study of Benvitimod cream in the treatment of chronic simple lichen

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096856
Enrollment
Unknown
Registered
2025-02-07
Start date
2024-09-25
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

Chronic simple lichen

Interventions

Benvitimod cream group:NA
Desonide cream group:NA

Sponsors

Taizhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) It meets the diagnostic criteria of chronic simple lichen, and is suitable for patients treated with Benvitimod cream; (2) Age >= 18 years old, = 8 points, of which the target lesion lichen like change score was >= 2 points, and the target lesion pruritus score was >= 2 points; (5) Women who were not pregnant and did not plan pregnancy during the trial; (6) Fully understand the content of the trial treatment, voluntarily participate in the trial treatment and have signed the informed consent; (6) Voluntarily participated in this observational study and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) Pregnant women, lactating women, or women preparing for pregnancy; (2) Known allergy to the active ingredients or excipients of the study drug; (3) Skin lesions with obvious exudation or accompanied by bacterial and fungal infections; (4) The patient may not be able to complete this study for other reasons, or the investigator believes that it is not appropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
Total skin lesion symptom score (TSS);

Secondary

MeasureTime frame
Eczema area and severity index,EASI;Dermatology quality of life index (DLQI);

Countries

China

Contacts

Public ContactChen Jinguang

Taizhou Central Hospital

chenjg@tzzxyy.com+86 135 6687 9800

Outcome results

None listed

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