NL-OMON20968
Recruiting
Not Applicable
A randomised, placebo controlled double blind study to assess the efficacy of a probiotic dairy product containing Lactobacillus casei Shirota on symptoms, visceroperception and inflammation in Irritable Bowel Syndrome.
Yakult Honsha Co. Ltd.1-19, 1 Chome, Higashi-ShinbashiMinato-ku 105-8660Tokyo JAPANContact person: Mr OosawaContact person in Europe: Dr S Kudo or Dr J Zhao, science managerScience department of Yakult Europe B.V.Yakult Europe B.V.Schutsluisweg 11332 EN ALMEREThe Netherlands0031(0)3652113000 sites60 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Irritable Bowel Syndrome (IBS) = Prikkelbare Darm Syndroom (PDS).probiotics = probioticacytokine profiles = cytokine profielenvisceroperception = visceroperceptielowgrade inflammation = laaggradige ontsteking
- Sponsor
- Yakult Honsha Co. Ltd.1-19, 1 Chome, Higashi-ShinbashiMinato-ku 105-8660Tokyo JAPANContact person: Mr OosawaContact person in Europe: Dr S Kudo or Dr J Zhao, science managerScience department of Yakult Europe B.V.Yakult Europe B.V.Schutsluisweg 11332 EN ALMEREThe Netherlands0031(0)365211300
- Enrollment
- 60
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
/A
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients will be included when:
- •1\. Diagnosed with IBS according to the ROME II criteria.
Exclusion Criteria
- •1\. Patients who have had gastrointestinal surgery resulting in gastric resection, small intestinal or colonic resection.
- •2\. Patients who are allergic to milk protein
Outcomes
Primary Outcomes
Not specified
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