Atopic Dermatitis Clinical Trial
Official title:
Collection of Clinical and Biometrological Data in Adult Subjects Suffering From Atopic Dermatitis (AD) During a Three-month Period
Atopic dermatitis represents a real challenge in public health as it affects a large
percentage of children and adults. Affected individuals must cope with a significant
psychosocial burden, in addition to dealing with the medical aspects of the disease.
The purpose of this exploratory study is to collect clinical severity AD data, using
PO-SCORAD (self-assessment by the subjects), SCORAD evolution, instrumental measurements and
treatment follow up of subjects.
The future objective is to develop a personalised prediction model of AD flares in order to
improve management of AD by more accurate severity evaluations by the subject and the
physician. Development of a method of early detection of flares will open new treatment
pathways for AD management.
This study will be conducted as a French monocentric exploratory study in adults with mild to
moderate Atopic Dermatitis, and will be conducted on a maximum 25 included subjects.
The clinical study will include 4 study visits, after inclusion visit, and the maximum
duration of the study for each subject will be 3 months : Day 1, Day 29, Day 57, Day 85.
In case of AD flare suspicion, the investigator may recommend a complementary visit. Any
complementary visit will be confirmed by investigator according to the subject's information:
photographs and PO-SCORAD sent by the subject. If visit is confirmed, it will be scheduled as
soon as possible.
The objectives are:
- to collect clinical AD severity data in order to evaluate natural AD evolution with
clinical and subject's scales, during a three-month period.
- to collect non-invasive instrumental AD data on a target area and on adjacent area:
cutaneous hydration, epidermal barrier conditions and colorimetric parameters on
cutaneous erythema
- to examine clinical and instrumental AD data
- to collect illustrative photographs of AD lesions
;
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