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Recruiting NCT07132333

Molecular Inflammation Board at the Center for Personalized Medicine

Observational Psoriasis (PsO) Psoriasis Arthritis Inflammatory Bowel Disease (Crohn's Disease and Ulcerative Colitis) Spondylarthropathies

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Biologic Agent.
Who it may be relevant to
Registry conditions: Psoriasis (PsO), Psoriasis Arthritis, Inflammatory Bowel Disease (Crohn's Disease and Ulcerative Colitis), Spondylarthropathies. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Germany
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Molecular Inflammation Board at the Centers for Personalized Medicine at the University Hospitals of Freiburg, Heidelberg, Tübingen and Ulm - A Multicenter Prospective Observational Study

Overview

Molecular Inflammation Board at the Center for Personalized Medicine

Detailed description

Molecular Inflammation Board at the Center for Personalized Medicine

The study objectives are:

To ensure a prospective documentation of all patients who are referred to the Molecular Inflammation Board in routine clinical care To prospectively ensure the documentation of MEB patients with an emphasis to clinical outcome parameters and further response assessments (e.g. peripheral immunmonitoring, imaging parameters) To prospectively assess patient-reported outcome of MEB patients To evaluate compliance to MEB suggestions in routine clinical care

Interventions

  • Biological Biologic Agent
    Intervention with biologic agents

Primary outcome measures

  • Therapy persistence [Time frame: Through study completion, an average of 1 year]

Eligibility criteria

Inclusion criteria

  • Chronic inflammatory disorder (PsO, PsA, SpA, IBD)
  • Given informed consent
  • 18 years of age

Exclusion criteria

  • No capacity to consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Germany · 1 center
  • University Hospital of Tübingen - Center for Personalized Medicine — Tübingen

Identifiers

NCT: NCT07132333 · 482/2022BO1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗