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Study on the microscopic characteristics of skin blood vessels in inflammatory skin diseases and the efficacy and safety of abrocitinib tablets combined with Crisborole ointment in the treatment of moderate to severe atopic dermatitis

Study on the microscopic characteristics of skin blood vessels in inflammatory skin diseases and the efficacy and safety of abrocitinib tablets combined with Crisborole ointment in the treatment of moderate to severe atopic dermatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097331
Enrollment
Unknown
Registered
2025-02-17
Start date
2023-10-30
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Atopic Dermatitis

Interventions

Prospective studies:The patient takes 100mg of Abrocitinib once daily and applies Crisaborole ointment twice daily for a duration of three months.

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Cross-sectional Study Inclusion Criteria (1) Diagnosis of atopic dermatitis. (2) No restrictions on nationality, gender, or ethnicity. (3) Willingness to cooperate in filling out clinical questionnaires. 2. Retrospective Study Inclusion Criteria (1) Patients who have already been treated with Abrocitinib tablets in combination with Crisaborole ointment for moderate-to-severe atopic dermatitis. (2) Treatment regimen: Oral Abrocitinib tablets 100mg daily combined with Crisaborole ointment twice daily. 3. Prospective Study Inclusion Criteria (1) Diagnosis of atopic dermatitis according to Hanifin-Rajka criteria, Williams criteria, or Zhang Jianzhong diagnostic criteria. (2) IGA score >=3, EASI score>=16, PP-PP-NRS score>=4, with severity classified as moderate-to-severe. (3) Patients who are currently receiving oral Abrocitinib tablets (100mg daily) combined with Crisaborole ointment (twice daily), or patients who are about to start this combination therapy.

Exclusion criteria

Exclusion criteria: 1. Cross-sectional Study Exclusion Criteria (1) Patients with critical illness, acute diseases, or severe mental disorders. (2) Patients with infections, pregnancy, childbirth, trauma, or other stress-related conditions. Patients with any systemic diseases or other active skin conditions that could affect the results of this study. 2. Retrospective Study Exclusion Criteria (1) History of using other JAK inhibitors. (2) Pregnancy, or history of hepatitis B, tuberculosis, HIV, or any chronic, opportunistic, or severe infections. 3. Prospective Study Exclusion Criteria (1) History of using other JAK inhibitors. (2) Pregnancy, or history of hepatitis B, tuberculosis, HIV, or any chronic, opportunistic, or severe infections.

Design outcomes

Primary

MeasureTime frame
Eczema Area and Severity Index;Investigator's Global Assessment;Peak pruritus numerical score;Dermatology Life Quality Index;Dermoscopic image background color;Scale color in dermoscopic images;Vascular morphology under low-power dermatoscope;Vascular morphology under high magnification dermatoscope;Vascular arrangement pattern under dermatoscope;Other vascular arrangement patterns under dermatoscope, such as the centripetal shape of peripheral vascular loops and the circular arrangement around hair follicles;Skin Moisture;Skin oiliness;

Secondary

MeasureTime frame
Transepidermal water loss;Skin elasticity;Skin pigmentation;Skin pH;

Countries

China

Contacts

Public ContactBai Yanping

China-Japan Friendship Hospital

zhi@tsinghua.edu.cn+86 139 1075 8509

Outcome results

None listed

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