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NCT05363904Completed

Atopic Dermatitis: Sub-Saharan Africa vs. Central Europe

Environmental Impact and Immune Responses in Atopic Dermatitis Patients in Central Europe and Sub-Saharan Africa: A Prospective Study

Source: ClinicalTrials.gov · Last updated 9 Jul 2025

Brief summary (registry, in English)

Many people are affected by atopic dermatitis (AD) worldwide. However, clinical studies on AD in Sub-Saharan Africa are rare and there is a lack of knowledge about possible differences in pathogenesis between European and African AD. This study will collect clinical and laboratory data with the aim to compare clinical characteristics and immune responses in AD patients in Sub-Saharan Africa and Central Europe. Furthermore, relevant allergens as well as the nasal, skin and gut micro- and mycobiome will be investigated.

Status (registry)
Completed
Study type
Observational
Enrollment
240 (actual)
First submitted
4 Mar 2022
Start date
30 Mar 2022
Primary completion date
12 Mar 2025
Lead sponsor
University of Zurich
NCT number
NCT05363904

What you commit to

  • Study type: Observational
  • Participants enrolled: 240
  • From 30 Mar 2022 to the primary completion date, 12 Mar 2025
  • 3 sites in 3 countries
  • 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 immunomodulatory/-suppressive treatment
    • Glucocorticoids or immunosuppressants (last 4 weeks) or
    • JAK inhibitors (last week) or
    • Omalizumab (last 4 weeks) or
    • Other biologicals e.g. dupilumab (last 2 months)
  • Systemic antibiotic, antimycotic or antiviral treatment 4 weeks prior to start
  • Phototherapy 4 weeks prior to start
  • Undergoing surgery in the last 2 months

Other illness

  • Known or suspected systemic immunosuppression because of disease
  • Clinical signs of active bacterial, fungal or viral infection
  • Infarction (e.g. stroke), embolism, or thrombosis in the last 2 months
  • Inability to follow the study procedures e.g. due to language problems, dementia etc. of the participant

Other

  • Active neoplasia

Who the study is looking for

  • AD patients:
  • Age: ≥18 years
  • Written informed consent given after information about the research project
  • Suffering from active atopic dermatitis
  • No active skin disease other than atopic dermatitis
  • No known active inflammatory disease other than atopic dermatitis/atopic diseases
    • HC participants:
  • Age: ≥18 years
  • Written informed consent given after information about the research project
  • No active skin disease
  • No known atopic disease (atopic dermatitis, asthma, allergy, allergic rhinoconjuncitivitis)
  • No known active inflammatory disease

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

Full criteria on ClinicalTrials.gov

Sites (3)

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

SiteCityCountrySite status
University Hospital Zurich
Coordinator of this site? Confirm its status
ZurichSwitzerlandUnknown status
University Hospital Joseph Raseta Befelatanana
Coordinator of this site? Confirm its status
AntananarivoMadagascarUnknown status
Regional Dermatology Training Centre (RDTC)
Coordinator of this site? Confirm its status
MoshiTanzaniaUnknown status

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