- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03633409
Differential EBI2 Expression Upon Allelic Status of the rs9557195 Polymorphism
Study Overview
Status
Conditions
Detailed Description
EBI2 is a risk gene for inflammatory bowel diseases (rs9557195). EBI2 is a G protein coupled receptors expressed on the immune cells. EBI2 directs migration and activity of immune cells.
Patients of the Swiss IBD cohort study have been genotyped for the allelic status of EBI2. The investigators will recruit patients with Crohn's disease and ulcerative colitis, assess epidemiological and clinical parameters (including clinical activity of IBD) draw blood, isolate lymphocytes, DNA and RNA.
The investigators will test the influence of rs9557195 genotype (TT or CC allel), inflammatory activity and current treatment (infliximab vs. vedolizumab) on expression and activity of EBI2 on blood lymphocytes (by FACS using an EBI2-antibody), mRNA expression (by qPCR) of EBI2 and UBAC2 (located on the opposite DNA strand of EBI2) and activity of lymphocytes on a migration assay.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Zurich, Switzerland, 8091
- Recruiting
- University Hospital Zürich
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Contact:
- Rene Roth, MD
- Phone Number: ++41 44 255 1111
- Email: rene.roth@usz.ch
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
we will recruit a mixed population (patients can be in more than one group)
- up to 100 healthy volunteers
- up to 30 IBD patients with the rs9557195-CC IBD risk genotype in clinical remission
- up to 30 IBD patients with the rs9557195-CT IBD risk genotype in clinical remission
- up to 30 IBD patients with the rs9557195-TT IBD low risk genotype in clinical remission
- up to 50 IBD patients of any genotype during a flare
- up to 50 IBD patients of any genotype treated with vedolizumab
- up to 50 IBD patients of any genotype treated with a TNF-inhibitor (infliximab, adalimumab, golimumab, certolizumab)
Description
Inclusion Criteria:
- Patient with IBD OR healthy volunteer
- No major uncontrolled medical/ surgical/ psychiatric condition requiring ongoing management besides IBD in the respective study groups. Well controlled conditions (i.e. medically controlled arterial hypertension, occupational asthma) may be present
Exclusion Criteria: none
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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IBD patients and healthy volunteers
We will recruit IBD patients and healthy volunteers
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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EBI2 expression - dependent on rs9557195 allele status (FACS)
Time Frame: at time of inclusion into the study
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EBI2 levels in PBMCs will be determined by FACS, and compared according to allele status of rs9557195
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at time of inclusion into the study
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
EBI2 expression - dependent on rs9557195 allele status (RT-PCR)
Time Frame: at time of inclusion into the study
|
EBI2 levels in PBMCs will be determined by RT-PCR, and compared according to EBI2 levels in PBMCs will be determined by RT-PCR, and compared according to allele status of rs9557195
|
at time of inclusion into the study
|
|
UBAC2 expression - dependent on rs9557195 allele status (RT-PCR)
Time Frame: at time of inclusion into the study
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UBAC2 levels in PBMCs will be determined by RT-PCR, and compared according to 2 levels in PBMCs will be determined by RT-PCR, and compared according to allele status of rs9557195
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at time of inclusion into the study
|
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Motility of PBMCs dependent on rs9557195 allele status (Boyden chamber)
Time Frame: at time of inclusion into the study
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motility of PBMCs will be assessed using the Boyden chamber and compared according to allele status of rs9557195
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at time of inclusion into the study
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EBI2-expression (FACS) in individuals treated with infliximab vs. vedolizumab
Time Frame: at time of inclusion into the study
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We will compare EBI2 expression as determined by FACS in individuals with infliximab and vedolizumab treatment
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at time of inclusion into the study
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EBI2-expression (FACS) according to gut inflammation
Time Frame: at time of inclusion into the study
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We will compare EBI2 expression (determined by FACS) in IBD patients with severe disease, in remission and in healthy volunteers
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at time of inclusion into the study
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- EBI2-Study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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