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Biobank for research into inflammatory diseases of the gastrointestinal tract

Biobank for research into inflammatory diseases of the gastrointestinal tract - iBiobank

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00035426
Enrollment
1000
Registered
2024-11-08
Start date
2024-10-09
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

K50-K52

Interventions

Group 1: Within the routine blood sampling, blood is also taken from patients for EDTA whole blood and serum collection and these samples are transferd to the biobank. Patients will also receive fecal

Sponsors

LMU Klinikum
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients (m/f/d) who are treated as inpatients, day inpatients, day patients, outpatients or consultants by the Medical Clinic and Polyclinic II of the LMU Hospital. The focus is on the inclusion of patients with IBD and other inflammatory diseases of the gastrointestinal tract.

Exclusion criteria

Exclusion criteria: Lack of consent for biobank participation.

Design outcomes

Primary

MeasureTime frame
The aim is to establish a prospective biobank to investigate the progression of inflammatory gastrointestinal diseases and their precursors. These included basic research as well as applied research for the detection of diseases (diagnosis), the prediction of their course (prognosis) as well as their treatment (therapy) and prevention (prevention). The purpose of the biobank is thus limited to a group of diagnoses and risk cohorts, but not to a single question or disease.

Secondary

MeasureTime frame
a) The recording, isolation and characterization of bacteria, archaebacteria, eukaryotes or viruses in the gastrointestinal tract (intestinal microbiome). b) Validation of liquid biopsy-based non-invasive tests for the early diagnosis and prediction of the course of diseases in at-risk patients. c) Identification and validation of new genetic risk variants, d) Evaluation of treatment strategies recommended in guidelines under "real-life" conditions. e) Comparison Biomaterials obtained from patients with samples from organoid cultures and mouse models with the aim of optimizing measurement methods and reducing animal experiments.

Countries

Germany

Contacts

Public ContactBenjamin Misselwitz

LMU Klinikum

benjamin.misselwitz@med.uni-muenchen.de+49 89 4400 75370

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026