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A controlled clinical study and safety assessment of abrocitinib in the treatment of erythrotelangiectasia rosacea

A controlled clinical study and safety assessment of abrocitinib and pimecrolimus in the treatment of erythrotelangiectasia rosacea

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093737
Enrollment
Unknown
Registered
2024-12-11
Start date
2024-02-29
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Erythrotelangiectasia rosacea

Interventions

half dose abrocitinib:Take one tablet of Abu Xitinib orally once a day for 4 weeks of treatment
pimcrolimus:Topical application of pimecrolimus once daily on the face for 4 weeks
full dose abrocitinib:Take Abuxitinib orally twice a day, one tablet each time, and treat for 4 weeks

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Women aged 18-60 with no cognitive impairment; 2) Rosacea with erythema telangiectasia that does not respond to traditional treatment (oral melamycin, topical tacrolimus) or relapsing; 3) After fully explaining the purpose and content of the clinical trial (including the subject's compliance, etc.), on the basis of full understanding, voluntarily sign the informed consent to participate in the clinical trial.

Exclusion criteria

Exclusion criteria: 1) Known allergy to the experimental drug or related drugs; 2) Received rosacea treatment (antibiotics, phototherapy, etc.) within 3 months before enrollment; 3) Patients with facial concomitations with other diseases that may affect the evaluation of efficacy (skin photosensitivity, porphyria, others) Photodermatosis, etc.); 4) Participate in any drug clinical trial (as a subject) within 1 month before participating in this trial; 5) Complicated with serious diseases, including severe heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled hyperemia Press and wait; 6) Patients with abnormal liver function, dyslipidemia or severe hypoimmunity; 7) Pregnant or lactating women, and participants of reproductive age (including men) who refused to use appropriate contraception during the study period; 8) Have a serious physical or mental illness that the investigator believes may affect treatment, evaluation, or protocol of the study Subjects with poor compliance.

Design outcomes

Primary

MeasureTime frame
efficacy propotion (erythema area);

Secondary

MeasureTime frame
a* value;erythema index;investigator global index;skin barrier function score;

Countries

China

Contacts

Public ContactXia Li

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

drlixia@126.com+86 21 64370045

Outcome results

None listed

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