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The TWIN study for Inflammatory Bowel Disease

Twin cohort for the study of (pre)clinical Inflammatory Bowel Disease in the Netherlands - The TWIN study - The TWIN study for Inflammatory Bowel Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON53107
Enrollment
444
Registered
2017-04-14
Start date
2017-09-11
Completion date
Unknown
Last updated
2025-09-08

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, ulcerative colitis

Interventions

Not applicable.

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
16 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for the IBD-discordant and IBD-concordant twins or multiples: - Born as a sibling of, either a monozygous or dizygous, twin pair or multiplex - One or more twin-siblings or multiples are affected with IBD, i.e. CD, UC or  IBD unspecified (self-reported diagnosis, to be confirmed during the study by  clinical, endoscopic or histological reports from the treating physician) - Age: 16 years and olderIn order to be eligible to participate in this  study, a subject must meet all of the following criteria for the unaffected  controls (preferably twins or multiples): - None of the siblings of the twin are affected with IBD, i.e. CD, UC or IBD  unspecified - Age: 16 years and older

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded  from participation in this study: - No consent to participate in the study. - Unable to read or understand the Dutch language.

Design outcomes

Primary

MeasureTime frame
Comparisons will be made between siblings of twin pairs and between IBD patients and non-IBD controls. Amongst others, changes in immune parameters in the mucosal and peripheral blood compartment, gut and oral microbiome, epithelium and mucus barrier function, and the metabolome will be studied. In addition, correlations between demographic, environmental and nutritional factors will be made, and quality of life an symptom fluctuations prior to or during IBD will be studied.

Secondary

MeasureTime frame
See above.

Countries

Netherlands

Contacts

Public ContactS.L. Dijkstra

Universitair Medisch Centrum Utrecht

s.l.dijkstra-6@umcutrecht.nl088-7550722

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)