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China Atopic Dermatitis Registry Study

Recruiting
Conditions
Dermatitis, Atopic
Interventions
Other: No intervention
Registration Number
NCT05023668
Lead Sponsor
Peking University People's Hospital
Brief Summary

This regestry study is aimed to characterize the medical care and drug treatment under real-life conditions among Chinese patients with moderate to severe Atopic Dermatitis who are not well controlled by topical therapies.

Detailed Description

Atopic dermatitis (AD) is a chronic recurrent inflammatory skin disease, resulting in itchy, red, and skin lesion. A survey conducted in 2014 in 39 tertiary hospitals of 15 provinces in mainland China has shown that the incidence of AD in outpatients (7.8%) has been raised in recent years.

Among topical therapy of AD, corticosteroids are first line therapy. In patients with extensive and severe dermatitis, topical therapy may be insufficient. Such patients may require the addition of either oral corticosteroid or systemic immunosuppressive therapy and even phototherapy. There is no clear recommendation treatment for each kind of patients with different severity yet and there are still huge unmet medical needs for treatment. There is not clear recommendation grade for these therapy in Chinese AD guideline and no published data to demonstrate current treatment situation in real clinical practise.

The goal of clinical registry study is to document the use and effectiveness of therapeutic interventions under real-life conditions. This study will help understand the clinical characteristics, treatment utilization, treatment patterns, as well as disease-related outcomes and cost among AD patients in China.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
10000
Inclusion Criteria
  • Age≥12;
  • AD according to Williams diagnosis criteria (see Appendix 1);
  • Moderate to severe AD that inadequately controlled by topical therapy
  • Moderate-to-severe: SCORAD score≥25; or
  • Inadequately controlled by topic therapies: Determined by physicians.
Exclusion Criteria
  • No.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Chinese moderate to severe atopic dermatitis patients not controlled by topical therapyNo interventionChinese moderate to severe atopic dermatitis patients not controlled by topical therapy
Primary Outcome Measures
NameTimeMethod
Patient-reported disease symptoms after Atopic Dermatitis therapies in real lifeAt Month 12

Patient Oriented Eczema Measure (POEM) will be used to assess disease symptoms

Physician evaluated effectiveness of Atopic Dermatitis therapies in real lifeAt Month 12

Physician-reported outcome tool, SCORAD index, will be used to evaluate the objective severity of clinical signs of Atopic Dermatitis .

Patient-reported severity of pruritus after Atopic Dermatitis therapies in real lifeAt Month 12

Peak Pruritus Numerical Rating Scale (NRS) will be used to assess severity of pruritus.

Patient-reported quality of life after Atopic Dermatitis therapies in real lifeAt Month 12

Dermatology Life Quality Index (DLQI) will be used to assess quality of life, and DLQI for children (cDLQL) will be used for adolescence patients.

Patient-reported disease control after Atopic Dermatitis therapies in real lifeAt Month 12

Atopic Dermatitis Control Tool (ADCT) will be used to assess long term disease control.

The Atopic Dermatitis related economic burdenAt Month 12

Economic burden of Atopic Dermatitis will be evaluated using the cost of hospitalizations and outpatient visits associated with Atopic Dermatitis during the past one year.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Peking University People's Hospital

🇨🇳

Beijing, Beijing, China

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