Actively Recruiting

Age: 0Years - 80Years
All Genders
Healthy Volunteers
ID05928169

Determinants of Chronic Inflammatory Skin Disease Trajectories

Led by University Hospital Schleswig-Holstein · Updated on 2025-07-22

1000

Participants Needed

1

Research Sites

35 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying chronic inflammatory skin diseases such as atopic dermatitis, psoriasis, and hidradenitis suppurativa, which show great variation in symptoms, severity, and treatment responses. The goal is to identify clinical and molecular factors that relate to disease subtypes and progression by closely following patients over a long period. This observational study aims to improve understanding of the natural course and variability of these conditions to help personalize patient care. Participants will be monitored through regular visits where clinical assessments and biological samples are collected. The study does not assign specific treatments but follows patients regardless of whether they use topical or systemic drugs. Evaluations occur at baseline, week 2, week 4, and then every three months for up to two years to capture changes in disease activity and molecular profiles over time. During the study, patients will undergo physician and patient assessments of disease activity, along with molecular testing from collected specimens. These measures are repeated regularly to track disease dynamics and flare-ups. The study includes safety considerations such as excluding recent use of certain immunosuppressive therapies. Participation can last up to two years, aiming to gather comprehensive data on disease progression and contributing factors.

CONDITIONS

Brief Title

Determinants of Chronic Inflammatory Skin Disease Trajectories

Who Can Participate

Age: 0Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Dermatologist-diagnosed inflammatory skin disease
  • Ability to provide informed consent
Not Eligible

You will not qualify if you...

  • Unable to provide written informed consent
  • Pregnant or breastfeeding women
  • Concurrent participation in another clinical trial
  • Use of systemic immunosuppressive therapy or phototherapy within the last 4 weeks
  • Receipt of biologic therapy (e.g., dupilumab, tralokinumab) within the last 3 months
  • Treatment of target skin areas with topical corticosteroids, calcineurin inhibitors, or emollients within 24 hours before sample collection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 2 years

Participants are observed over time with repeated clinical assessments and specimen collections to study the progression and molecular characteristics of their inflammatory skin disease.

Baseline, week 2, week 4, and every 3 months visits up to 2 years

Trial Site Locations

Total: 1 location

1

Department of Dermatology and Allergy, University Hospital Schleswig-Holstein

Kiel, Germany, 24105

Actively Recruiting

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Research Team

S

Stephan Weidinger, MD

S

Stefanie Sievers

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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