Staphylococcal Toxins in Atopic Dermatitis and Eczema Herpeticum

  • STATUS
    Recruiting
  • End date
    Oct 16, 2023
  • participants needed
    80
  • sponsor
    Poitiers University Hospital
Updated on 5 February 2021

Summary

Atopic dermatitis (AD) is the most common chronic inflammatory skin disease. Clinical studies have demonstrated a link between staphylococcal skin colonization and the pathogenesis of AD, but the implication of bacterial virulence factors remains largely uncharacterized. Finally, AD is often associated with herpes simplex skin infections. The aim of this project is to investigate the role of staphylococcal toxins in the exacerbation and maintenance of atopic skin inflammation and in the occurrence of infectious complications such as eczema herpeticum.

Details
Condition bacterial toxin, Eczema, Eczema (Atopic Dermatitis - Pediatric), Staphylococcus aureus, cytokine, ATOPIC DERMATITIS, Eczema (Atopic Dermatitis), ATOPIC DERMATITIS, Dermatitis, Atopic, Dermatite Atopique, Eczéma (Dermatite Atopique), Dermatitis, Hand Dermatitis, Eczema (Atopic Dermatitis), Dermatitis, Atopic, Hand Dermatitis, Eczema (Atopic Dermatitis - Pediatric), Immune Response, Eczéma (Dermatite Atopique), Dermatite Atopique, s. aureus, cytokines, T Cells Subsets
Treatment Skin biopsies and blood samples
Clinical Study IdentifierNCT04274348
SponsorPoitiers University Hospital
Last Modified on5 February 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients with moderate AD (SCORAD between 25 and 50) or severe AD (SCORAD> 50)
Skin lesions in the forearms
Free subject, without neither guardianship, wardship nor subordination
Patient with Social Security
Informed and signed consent by the patient after clear and loyal information on the study

Exclusion Criteria

Age < 18 year-old
Patients with mild AD (SCORAD < 25)
Patients without skin lesions in the forearms
Patients treated with dermocorticoid or calcineurin inhibitor for less than two weeks
Patients under systemic treatment : Methotrexate, Ciclosporin, Mycophenolate Mofetil, Azathioprine, general corticosteroids for less than 4 weeks
Patients under biological treatment : Dupilumab for less than 5 half-lives
Patient without Social Security
Pregnant and nursing women
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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