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Molecular Inflammation Board at the Center for Personalized Medicine

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07132333
Acronym
MEB@ZPM
Enrollment
3000
Registered
2025-08-20
Start date
2022-11-16
Completion date
2032-11-30
Last updated
2025-08-20

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

Conditions

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

Keywords

chronic inflammatory diseases, personalized medicine

Brief summary

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

BIOLOGICALBiologic Agent

Intervention with biologic agents

Sponsors

University Hospital Freiburg
CollaboratorOTHER
University Hospital Heidelberg
CollaboratorOTHER
University Hospital Ulm
CollaboratorOTHER
University Hospital Tuebingen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

* No capacity to consent

Design outcomes

Primary

MeasureTime frameDescription
Therapy persistenceThrough study completion, an average of 1 yearDuration of intervention with biological agent

Countries

Germany

Contacts

Primary ContactNisar P Malek, Prof. Dr.
zpm-meb@med.uni-tuebingen.de+4970712982722

Outcome results

None listed

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