Filaggrin mutation polymorphism
Conditions
Interventions
None listed
Sponsors
Vrije Universiteit Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Written informed consent Age 18 to 70 Legally competent adults Inclusion in fragrance study
Exclusion criteria
Exclusion criteria: Severe illness, defined as life threatenig of severely disabling
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study parameters are: Objective 1&2: -Mean patch test reactions on SLS in 0%, 0.45%, 0.67%, 1% and 1.5% in water solution in TEWL (derived from *fragrance study*) This is a continuous numerical data. Objective 3 &4: -ACD The endpoints are: -Presence or absence of a mutation for fillagrin and/or specific cytokines (such as interleukin (IL)-1*, IL-1*, IL-8, IL-10, and eventually other relevant cytokines, dependent on future developments) -Atopy scoring through questionnaires -Demographic data of the population (gender, age, etc.) | — |
Countries
Netherlands
Outcome results
None listed