Actively Recruiting
Goat vs. Cow Milk Digestive Tolerance
Led by Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · Updated on 2025-11-20
20
Participants Needed
1
Research Sites
70 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of this study is to assess to what extent goat's milk is better tolerated than cow's milk among individuals who report being intolerant to cow's milk, and, if so, to understand the underlying factors. To achieve this, digestive discomfort sensations and postprandial kinetics of nutrients after ingestion of cow's or goat's milk will be compared in two populations: individuals intolerant to cow's milk but not to goat's milk, and individuals who show no symptoms of intolerance to either cow's or goat's milk. For this purpose, approaches based on stable isotope labeling of milk will be employed.
CONDITIONS
Official Title
Goat vs. Cow Milk Digestive Tolerance
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals who report being intolerant to cow milk but not to goat milk or tolerant to both cow milk and goat milk
- Good general health (WHO grade = 0)
- Affiliated with a social security scheme
- Free, informed, and express consent in accordance with the public health code
You will not qualify if you...
- Individuals under guardianship, curatorship, or legal protection
- Any known food allergies
- Anemia with hemoglobin below 13 g/dL for men or 12 g/dL for women
- Pregnant women or those likely to be pregnant based on a urine pregnancy test
- Excessive alcohol consumption (more than 2 drinks per day)
- Hypertension, diabetes, digestive tract diseases (except irritable bowel syndrome), liver or kidney diseases, severe heart disease
- Elite athletes training more than 8 hours per week
- Blood donation in the 3 months before the study
- Participation in another clinical study in the 3 months before the study
- Lack of free, informed, and express consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Hôpital Avicenne, 125 rue de Stalingrad
Bobigny, France, 93000
Actively Recruiting
Research Team
S
Saviard
CONTACT
M
Maurinier
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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