Fact CheckerSign in

NCT06455891Completed

MYCobiome Analysis in Atopic Dermatitis With Head and Neck Involvement

Source: ClinicalTrials.gov · Last updated 11 Mar 2026

Brief summary (registry, in English)

It is an open study, explorative, proof of concept study concerning mycobiota dysbiosis implication in AD patients with head and neck involvement.

Status (registry)
Completed
Study type
Observational
Enrollment
30 (actual)
First submitted
7 May 2024
Start date
May 2024
Primary completion date
Dec 2025
Lead sponsor
Assistance Publique - Hôpitaux de Paris
NCT number
NCT06455891

What you commit to

  • Study type: Observational
  • Participants enrolled: 30
  • From May 2024 to the primary completion date, Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Systemic or local antifungal therapy within 2 months before entry and during the study
  • Systemic treatments for AD; including: ciclosporine, dupilumab and others AD biologics, methotrexate, JAK-inhibitors
  • Psychiatric illness or any other concomitant chronic illness or addiction that could be interfere with the ability to meet the requirements of the protocol or provide informed consent

Other

  • Current participation in another interventional research
  • Patient with a measure of legal protection

Who the study is looking for

  • Age between 18 and 65 years;
  • Male or female;
  • The diagnosis of atopic dermatitis (AD) is defined according to the criteria of UK Working Party with at least 3 of the following 5 criteria are present; history of flexural involvement, history of a dry skin, onset under the age of 2, personal history of asthma or allergic rhinitis, history of a pruritic skin condition, and visible flexural dermatitis.
  • Generalized AD defined by AD involved ≥50% of total body surface area with head and neck involvement. Or HNAD defined by AD involving at least 80% of the head and neck area with or without AD involvement outside the head and neck area but \<20% of total body surface area.
  • With or without topical anti-inflammatory treatments for AD (including; topical steroids and/or topical tacrolimus)
  • Free, informed and written consent, signed by the patient and the investigator before any examination required by the trial;
  • Affiliation to social security scheme (beneficiary or assignee)
  • Healthy control are the same age and sex.

Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tenon Hospital APHP dermatology and allergology department
Coordinator of this site? Confirm its status
ParisFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.