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Staphylococcal Toxins in Atopic Dermatitis and Eczema Herpeticum (STADEH)

P

Poitiers University Hospital

Status

Completed

Conditions

Atopic Dermatitis
Immune Response
Cytokines
Bacterial Toxins
T Cells Subsets
Staphylococcus Aureus

Treatments

Other: Skin biopsies and blood samples

Study type

Interventional

Funder types

Other

Identifiers

NCT04274348
2019-A01904-53

Details and patient eligibility

About

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.

Enrollment

41 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

41 participants in 1 patient group

Skin biopsies and blood samples
Other group
Treatment:
Other: Skin biopsies and blood samples

Trial contacts and locations

2

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Central trial contact

Ewa HAINAUT, Dr

Data sourced from clinicaltrials.gov

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