IBS - Irritable Bowel Syndrome Clinical Trial
— PN-AI-21Official title:
Microbiota, Metabolome and Nutrition: an 'Artificially Intelligent' Way to Personalized Nutrition
Intervention: (Weeks 1-2, Visit 3-4) - Starting from the second week after the date of consent, patients with IBS will be randomized 1:1 into two groups. The first group (20 patients) will receive one week of a low FODMAP supplemented with fermented milk followed by one week of a low FODMAP content supplemented with fermented beans. The second group (20 patients) will receive a low FODMAP diet supplemented for one week with fermented beans followed by a second week of a diet with a low FODMAP diet supplemented with fermented milk. The microbiome of the patients will be evaluated after the first and second weeks along with data related to weight. After the second week, the metabolome and physical characteristics. The enrollment period will last for one year. The analysis of clinical data will be completed within one year after patient enrollment. Analysis of laboratory data will be performed in parallel.
Status | Recruiting |
Enrollment | 48 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - Patients of both sex and any race - Age =18 and =70. - IBS confirmed by Rome IV diagnostic criteria - Willing to adhere to the proposed diet - Provision of written informed consent - Commitment of availability throughout the study period Exclusion Criteria: - Patient age <18 and > 70 - Diabetes (Type 1 or 2) - Subjects who have used probiotic, antibiotic, lactic ferment or pump inhibitors within 15 days prior to screening. - Pregnant or planning to become pregnant or is lactating. - History of HIV or hepatitis B or C - Participation in investigational study within past 30 days - Unstable cardiovascular or pulmonary disease, with change in treatment in last 30 days due to worsening disease condition - Any concomitant disease requiring specialized nutrition (e.g. renal failure, celiac disease, cerebrovascular disease of the central nervous system, major surgical cavity) |
Country | Name | City | State |
---|---|---|---|
Italy | Endoscopy Unit, Gastroenterology Department, Humanitas Research Hospital | Rozzano | Milano |
Lead Sponsor | Collaborator |
---|---|
Istituto Clinico Humanitas |
Italy,
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* Note: There are 28 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Microbiome | The primary endpoint will be the change in the phenotype of microbiome and metabolome in the two-study group at the end of the assumption of fermented food. Stool samples will be thoroughly analyzed for microbiome (amplified for 16S rDNA sequencing and/or shotgun) and metabolome composition (untargeted). IBS-related symptoms will also be evaluated at the end of one week of low FODMAP diet consumption. | 1 week | |
Secondary | Microbiome after baseline | to assess and compare the changes in the microbiome and metabolome phenotype at baseline and 1 week after the low FODMAP diet assumption, and after 1 week of addition of fermented food.Patients' microbiome will be assessed after the first and second week by collecting a fecal sample together with data regarding the weight. Metabolome and IBS-related symptoms will be evaluated in a longitudinal study after the second week as previously mentioned. | 2 weeks | |
Secondary | GSRS score | to assess and compare any change in the GSRS score at baseline, after 1 week of low FODMAP diet assumption and at the end of the study in the two study groups.
GSRS is a symptom assessment tool that measures the baseline severity and frequency of these symptoms, as well as the response to treatment(1). |
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