Irritable Bowel Syndrome Clinical Trial
Official title:
A Randomized Controlled Clinical Trial to Investigate the Efficacy of Lacto-fermented Sauerkraut and the Probiotic E. Coli Nissle 1917 in the Treatment of Irritable Bowel Syndrome
The aim of the present study is to assess the efficacy of two different probiotic products, lacto-fermented sauerkraut and the supplement Mutaflor, in the treatment of irritable bowel syndrome.
Status | Recruiting |
Enrollment | 140 |
Est. completion date | July 2017 |
Est. primary completion date | July 2017 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 16 Years to 65 Years |
Eligibility |
Inclusion Criteria: Rome III criteria (Criteria fulfilled for the last 6 months with symptom onset at least 3 months prior to diagnosis): Recurrent abdominal pain or discomfort at least 3 days/month in the last 3 months associated with two or more of the following: 1. Improvement with defecation 2. Onset associated with a change in frequency of stool 3. Onset associated with a change in form (appearance) of stool Exclusion Criteria: - Psychiatric disorder - Metabolic disease - Chronic infection - Organic gastrointestinal disorder - Pregnancy - Breastfeeding |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Norway | Volvat Medisinske Senter, Majorstuen | Oslo |
Lead Sponsor | Collaborator |
---|---|
University of Copenhagen |
Norway,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | IBS Symptom Severity Scale (IBS-SSS). | Change from day 0 to day 42 | No | |
Secondary | Body weight | Change from day 0 to day 42 | No | |
Secondary | Fecal microbiome diversity | 16S rRNA gene sequences (prokaryotes) | Change from day 0 to day 42 | No |
Secondary | The Quality of Life Scale (QOLS) | Change from day 0 to day 42 | No |
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