Maastricht IBS Cohort: Phenotypical and genotypical characterization of patients with Irritable Bowel Syndrome
- Conditions
- Irritable bowel syndrome10017977
- Registration Number
- NL-OMON50635
- Lead Sponsor
- Interne Geneeskunde
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 1400
IBS patients:
1) IBS will be diagnosed according to the Rome III criteria:
Recurrent abdominal pain or discomfort at least 3 days per month in the last 3
months associated with 2 or more of the following:
* Improvement with defecation
* Onset associated with a change in frequency of stool
* Onset associated with a change in form (appearance) of stool
2) Based on the medical history and previous examination, no other causes for
the abdominal complaints can be defined. , Healthy controls:
1) Age between 18 and 75 years
IBS patients:
1) Abdominal surgery, except for uncomplicated appendectomy, laparoscopic
cholecystectomy or hysterectomy. , Healthy controls:
1) Gastrointestinal disorders (current or in medical history) or current
gastrointestinal complaints.
2) Abdominal surgery, except for uncomplicated appendectomy, laparoscopic
cholecystectomy or hysterectomy.
3) Use of medication that can influence gastrointestinal motility or perception
(like loperamide, butylscopolamine, psylliumsead (metamucil), duspatal,
metoclopramide, domperidon, erytromycine and serotonin reuptake inhibitors),
for at least 3 months before tests.
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Hypothesis:<br /><br>Subgroups of IBS patients can be identified according to phenotypical and<br /><br>genotypical patterns<br /><br><br /><br>Primary objective:<br /><br>- To set up a cohort of at least 1000 IBS patients and 400 healthy controls in<br /><br>order to identify different patient subgroups according to phenotypical and<br /><br>genotypical patterns</p><br>
- Secondary Outcome Measures
Name Time Method