The primary objective of the present multicentre, prospective, non-interventional study (NIS) is gathering knowledge on the actual use and effectiveness of Elidel® in Chinese patients with mild to moderate AD affecting sensitive skin areas in routine clinical practice.
Study Type
OBSERVATIONAL
Enrollment
130
Elidel® as prescribed within routine clinical practice
Beijing children's Hospital, Capital Medical University
Beijing, China
Beijing Hospital
Beijing, China
Children's Hospital Capital Institute of Pediatrics
Beijing, China
Peking University First Hospital
SCORAD
The primary outcome measure is the "change from baseline in SCORAD INDEX". The achievable score in SCORAD INDEX range from 0 to 103. The classification of severity would be as follows mild (\<25), moderate (25-50) and severe (≥50).
Time frame: The study ends after the Maintenance Period of at least 3 months allowing certain flexibility to respond to the routine practice. End of Study will be approx. 6 months after the inclusion depending length of the Elidel® Treatment Period.
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Beijing, China
Peking University Third Hospital
Beijing, China
Children's hospital of Chongqing medical university
Chongqing, China
The third affiliated hospital, sun yat-sen university
Guangzhou, China
The first Hospital of China Medical University
Shenyang, China
Peking University Shenzhen Hospital
Shenzhen, China
Tongji Medical College Huazhong University of Science & Technology
Wuhan, China