Visceral Sensitivity in IBD and IBS: Role of Inflammation, Immune Activity and Genetic Factors

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Aim: More insight in pathogenesis of IBS and IBD. Samples are collected in context of an European research project.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: t
View:

⁃ For group 1: IBS

• Irritable Bowel Syndrome (IBS) (ROME III criteria)

• No obvious organic explanation for the IBS symptoms

• Medication which affects the gastrointestinal motility or perception should be stopped at least 24 hours before the study

⁃ 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)

• diagnosis of Crohn's disease (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

Locations
Other Locations
Belgium
University Hospitals Leuven
RECRUITING
Leuven
Contact Information
Primary
Koen Bellens, MSc
koen.bellens@kuleuven.be
0032-16-341943
Time Frame
Start Date: 2010-02
Estimated Completion Date: 2099-01
Participants
Target number of participants: 99999999
Treatments
Other: Sample collection
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
Sponsors
Leads: KU Leuven

This content was sourced from clinicaltrials.gov