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In depth characterization of the mucosal microbiota in patients with IBD using novel, potent high-throughput approaches and their interaction with the immune system

In depth characterization of the mucosal microbiota in patients with IBD using novel, potent high-throughput approaches and their interaction with the immune system - Microbiota and immune cells in IBD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36766
Enrollment
88
Registered
2011-11-08
Start date
2011-11-11
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Crohn's disease Inflammatory Bowel Disease Ulcerative Colitis

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: *18 year old male or female, able to give informed consent Established Crohn*s disease or ulcerative colitis (according to the Lennard-Jones criteria), or patients scheduled for diverting ostomy due to IBD. control patients: patients who undergo intestinal resection due to a gastrointestinal malignancy

Exclusion criteria

Exclusion criteria: Ischemia of the bowel Positive stool cultures or parasite tests for common enteric pathogens (with exeption of non pathogenic parasites such as Blastocystis hominis or Endolimax nana) Use of Antiobiotics in preceding 4 weeks use of probiotics in preceding 8 weeks

Design outcomes

Primary

MeasureTime frame
- Nature and transmural spatial distribution of the enteric microbiota in IBD patients. - Changes in mucosal microbiota of the sigmoid in IBD after diverting ostomy. - Phenotype and characterise the immune cells involved in IBD.

Secondary

MeasureTime frame
- Presence of microbial DNA in granuloma*s of CD patients. - Assessment of co-localisation and signalling between invading microbes, lamina propria macrophages dendritic cells and adaptive and innate immune cells. - Alterations of phagosome maturation and autophagy, as well as apoptosis of mucosal macrophages and dendritic cells in IBD.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)