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Aim:
More insight in pathogenesis of IBS and IBD. Samples are collected in context of an European research project.
Methods:
Sample collection in healthy subjects, IBD and IBS patients:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Sample collection | Other | Collection of blood, feces samples, sample of nasal mucosa and biopsies (rectum and colon descendens), questionnaires and performance of rectal sensitivity measurement (barostat), MR scan of brain and transit measurement of colon |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Sample collection | Other | Collection of blood, feces samples, sample of nasal mucosa and biopsies (rectum and colon descendens), questionnaires and performance of rectal sensitivity measurement (barostat), MR scan of brain and transit measurement of colon |
| Measure | Description | Time Frame |
|---|---|---|
| differences in visceral sensitivity in different study groups (Visceral sensitivity will me measured by performing a rectal barostat test) | Visceral sensitivity will me measured by performing a rectal barostat test | at time of investigation (rectal barostat test), Day 1 |
| Measure | Description | Time Frame |
|---|---|---|
| immune activity (measuring release of mest cell mediators in rectal biopsies, measuring parameters of immune activity in blood) | measuring release of mest cell mediators in rectal biopsies, measuring parameters of immune activity in blood (for example by stimulating Peripheral Blood Mononuclear Cells) | at time of investigation (rectal biopsy), Day 1 |
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Inclusion Criteria:
For group 1: IBS
Group 2: active ulcerative colitis 1. diagnosis of ulcerative colitis (Confirmed by at least one sigmoidoscopy) 3. Medication which affects the gastrointestinal motility or perception should be stopped at least 24 hours before the study
Group 3: ulcerative colitis in remission (3a: with IBS symptoms, 3b: without IBS symptoms)
diagnosis of ulcerative colitis (Confirmed by at least one sigmoidoscopy)
remission is confirmed by at least one sigmoidoscopy
Medication which affects the gastrointestinal motility or perception should be stopped at least 24 hours before the study
Only for group 3a:
Rome III criteria for IBS
Group 4: Healthy controls No abdominal (pain) complaints.
Group 5: active Crohn's disease
1. diagnosis of Crohn's disease (Confirmed by at least one sigmoidoscopy) 3. Medication which affects the gastrointestinal motility or perception should be stopped at least 24 hours before the study
Group 6: Crohn's disease in remission (6a: with IBS symptoms, 6b: without IBS symptoms)
Exclusion Criteria:
For all groups:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Koen Bellens, MSc | Contact | 0032-16-341943 | koen.bellens@kuleuven.be |
| Name | Affiliation | Role |
|---|---|---|
| Guy Boeckxstaens, MD | Catholic University Leuven and Universitary Hospitals Leuven | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospitals Leuven | Recruiting | Leuven | Vlaams-Brabant | 3000 | Belgium |
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| ID | Term |
|---|---|
| D003093 | Colitis, Ulcerative |
| D009043 | Motor Activity |
| D003424 | Crohn Disease |
| ID | Term |
|---|---|
| D003092 | Colitis |
| D005759 | Gastroenteritis |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D015212 | Inflammatory Bowel Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D001519 | Behavior |
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| ID | Term |
|---|---|
| D013048 | Specimen Handling |
| ID | Term |
|---|---|
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
| D008919 | Investigative Techniques |
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