Skip to content

Disease Trajectories and Anti-cytokine Response Signatures in Atopic Dermatitis and Psoriasis

Disease Trajectories in Atopic Dermatitis and Psoriasis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03361215
Acronym
DiTrAP
Enrollment
1000
Registered
2017-12-04
Start date
2015-03-16
Completion date
2030-12-31
Last updated
2025-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atopic Dermatitis, Healthy, Psoriasis

Keywords

Disease progression, Disease course, Immunological characterization

Brief summary

The clinical study investigates the long-term course of disease in patients with chronic inflammatory skin diseases (atopic eczema and psoriasis) and the impact of tarheted therapies on the clinical and molecular level. For this purpose, patients are asked to take part in regular examinations and data collections, and to donate biomaterials (blood, skin biopsies, skin swabs, tape strips, stool samples). Blood samples are used to analyze inflammation messengers. Punch biopsies from lesional and non-lesional skin areas are used to analyze gene expression. Tape strips are pieces of transparent adhesive tapes to strip off most of the horny layer that will be used to examine mRNA and protein expression. The skin smears are superficial smears of three areas of skin with cotton swabs, which are used to examine bacteria on the skin. Overall, the study will help to monitor the disease course clinically and on the molecular level in participating patients for at least ten years and to collect information about the impact of various external factors including treatments. The study has no effect on the therapies of the disease, it serves only the accompanying data collection

Detailed description

Atopic dermatitis and psoriasis are the most common chronic inflammatory skin diseases in dermatology. Due to genetic predispositions, inflammatory changes of the skin occur. The specific mechanisms are only partly understood for both diseases and targeted therapies are established in psoriasis therapy and are becoming available for atopic dermatitis. In order to better understand the course of the disease and to characterize the changes in the inflammatory mechanisms during the course of the disease and under the influence of external factors such as therapies, longitudinal prospective studies are needed to evaluate clinical data and biological samples. This study investigates long-term clinical and epidemiological data from affected patients, as well as biological samples, including blood samples, skin biopsies, non-invasive skin swabs for microbiome detection, and tape strips for the molecular characterization of the disease. Data collection and biosampling will be done during routine visits, typically at week 0, 2, 4, 12 and 52.

Interventions

OTHERBiosampling for molecular analysis

Observational study with no therapeutic intervention. Biosampling for molecular analysis

Sponsors

University Hospital Schleswig-Holstein
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients with a clinical diagnosis of atopic dermatitis, psoriasis or autoimmune skin disease * Written informed consent obtained from the subject

Exclusion criteria

* Patients who decline participation In patients\<18 years of age no biopsies will be taken

Design outcomes

Primary

MeasureTime frameDescription
Disease progression10 yearsEpidemiological and phenotypical data of patients
Molecular signature changes10 yearsMolecular signatures will be measured using OMICS and sequencing technologies

Secondary

MeasureTime frameDescription
Development of comorbidities10 yearsAssessment of newly developed comorbid diseases over time

Countries

Germany

Contacts

Primary ContactStephan Weidinger, Prof. Dr.
sweidinger@dermatology.uni-kiel.de+49431500
Backup ContactSascha Gerdes, PD Dr.
sgerdes@dermatology.uni-kiel.de+49431500

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026