Skip to content

A Prospective Cohort Study on the Clinical and Molecular Heterogeneity of Atopic Dermatitis

A Prospective Cohort Study on the Clinical and Molecular Heterogeneity of Atopic Dermatitis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116197
Enrollment
Unknown
Registered
2026-01-06
Start date
2025-08-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Atopic dermatitis

Interventions

Moderate-to-Severe AD (Biologics or JAK Inhibitor Treatment Group):None
AD (Non-biologics or JAK Inhibitor Treatment Group):None

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Meeting the Chinese diagnostic criteria for atopic dermatitis (Electronic Medical Record Registration Study and Prospective Cohort Study on Moderate to Severe AD); 2.No age or gender restrictions (Electronic Medical Record Registration Study); 3.Voluntarily sign the informed consent form (Electronic Medical Record Registration Study and Prospective Cohort Study on Moderate to Severe AD); 4.Age >= 12 years (Prospective Cohort Study on Moderate to Severe AD); 5.Candidates for treatment with biologic agents or JAK inhibitors (Prospective Cohort Study on Moderate to Severe AD); 6.At the baseline visit, IGA >= 3 (on the 0-4 IGA scale, where 3 is moderate and 4 is severe) or EASI >= 7 (Prospective Cohort Study on Moderate to Severe AD);

Exclusion criteria

Exclusion criteria: 1.Unwillingness to sign the informed consent form;

Design outcomes

Primary

MeasureTime frame
The proportion of subjects who achieved EASI-75 at Week 48;The proportion of subjects who achieved EASI-75 at Week 12;

Secondary

MeasureTime frame
Proportion of subjects with IgA score of 0 or 1 and a decrease of >= 2 points from baseline;Proportion of subjects whose IgA score decreased by >= 2 points from baseline;Proportion of subjects reaching easi-90 and easi-50;Proportion of subjects whose pp-nrs decreased by >= 4 points from baseline;Easi change from baseline and percentage change;ADCT change from baseline and percentage change;

Countries

China

Contacts

Public ContactGu Chaoying

Huashan Hospital, Fudan University

2269718228@qq.com+86 21 52887783

Outcome results

None listed

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