Irritable Bowel Syndrome Clinical Trial
Official title:
Impact of A2 Milk Versus Conventional Milk on Intestinal Health: a Proof-of-concept Study in Irritable Bowel Syndrome Patients
Verified date | January 2024 |
Source | Maastricht University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This aim of this study is to evaluate the acute and mid-term effects of A2 milk versus conventional milk on gastrointestinal symptoms in patients with constipation-predominant IBS and in patients with diarrhea-predominant IBS. Moreover, the effect of immune and defense markers will be studied.
Status | Completed |
Enrollment | 10 |
Est. completion date | June 5, 2023 |
Est. primary completion date | June 5, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility | Inclusion Criteria: - IBS with constipation (IBS-C) or IBS with diarrhea (IBS-D), based on the Rome IV criteria - Self-reported indication that dietary components (e.g. milk) trigger GI symptoms - Body Mass Index (BMI) < 30 kg/m2 - Weight-stable for at least 90 days prior to participation (no change in bodyweight, i.e. < 3kg). - Willing to be informed in case of unexpected findings. Exclusion Criteria: - History of any disease or surgery interfering with the study aims, limiting participating or completing the study protocol - Self-admitted human immunodeficiency virus-positive state. - Disease with a life expectancy shorter than 5 years. - Abdominal surgery interfering with gastrointestinal function (to be decided by a medical doctor) - Based on anamnesis, patients with lactose intolerance will be excluded. If not tested before, a lactose breath test can be performed to check for lactose intolerance. - Self reported cow's milk allergy - Use of antibiotics within 30 days prior to the study - Use of other medication interfering with study outcomes, as will be reviewed by a medical doctor, who will decide on in- or exclusion based on the drug(s) used - Administration of probiotic or prebiotic supplements, investigational drugs or participation in any scientific intervention study, which may interfere with this study (to be decided by the principle investigator), in the 14 days prior to the study - Known pregnancy or lactation - Plan to loose weight or follow a specific diet within the study period - Alcohol intake: female >7 units/week for females, male >14 units/week - Blood donation within 1 month prior to the study - Insufficient fluency of the Dutch language |
Country | Name | City | State |
---|---|---|---|
Netherlands | Maastricht UMC+ | Maastricht | Limburg |
Lead Sponsor | Collaborator |
---|---|
Maastricht University Medical Center |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The acute effects of A2 milk versus conventional milk on overall gastrointestinal discomfort in separate groups of individuals with IBS-C and IBS-D. | Assessed by a single item using a visual analogue scale (VAS), anchored at the low end (score of 0) with the absence of overall symptoms and at the other end (score of 100) with severe symptoms, the worst it has ever been. | On the 1 day intervention period | |
Secondary | The mid-term effects of A2 milk versus conventional milk on overall gastrointestinal discomfort in separate groups of individuals with IBS-C and IBS-D. | Assessed by a single item using a visual analogue scale (VAS), anchored at the low end (score of 0) with the absence of overall symptoms and at the other end (score of 100) with severe symptoms, the worst it has ever been. | up to 3 days (once daily) after 1 day of intervention | |
Secondary | The acute and mid-term effects of A2 milk versus conventional milk on single gastrointestinal symptoms and stool characteristics in separate groups of individuals with IBS-C and IBS-D. | Assessed by a visual analogue scale (VAS) for different gastrointestinal symptoms, anchored at the low end (score of 0) with the absence of overall symptoms and at the other end (score of 100) with severe symptoms, the worst it has ever been. | Multiple times at the 1 day intervention day and once daily up to 3 days after intervention day | |
Secondary | The mid-term effects of A2 milk versus conventional milk on single gastrointestinal symptoms and stool characteristics in separate groups of individuals with IBS-C and IBS-D. | Assessed by the IBS-SSS questionnaire (a 0-100 scale, with the total IBS-SSS score ranging between 0 and 500, with higher scores indicating more severe symptoms). | At the first intervention day | |
Secondary | The mid-term effects of A2 milk versus conventional milk on gastrointestinal immune and defense markers in separate groups of individuals with IBS-C and IBS-D. | Assessed by several parameters of GI immune and defense in feces. | At both intervention days |
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