Healthy subjects
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy subjects who give informed consent to participate in the study and fulfill the eligibility criteria according to ISO26642 and study protocol
Exclusion criteria
Exclusion criteria: - Aged 60 years; - Pregnant or lactating; - Body mass index (BMI) 30 kg/m2; - Known history of diabetes mellitus or fasting blood glucose value > 6.1 mmol/l or the use of anti-hyperglycaemic drugsor insulin to treat diabetes and related conditions; - Any known food allergy or intolerance; - Medical condition(s) or medication(s) known to affect glucose regulation, tolerance or appetite and/or which influencedigestion and absorption of nutrients (excluding oral contraceptives); - Major medical or surgical event requiring hospitalization within the preceding 3 months; - Use of steroids, protease inhibitors, amphetamines or antipsychotics (all of which have major effects on glucosemetabolism and body fat distribution); - Suspicion of alcohol abuse (defined as an average daily intake of more than 6 units of alcohol per day, e.g. more than 2 pints of beer per day or equivalent amount of alcohol in other beverages) or drug abuse; - Participants who are unable to comply with experimental procedures or do not follow GI testing safety guidelines or are not able to tolerate fasting condition for at least 10 hours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Glycaemic index (GI). Blood samples will be taken at -5 min and 0 min before consumption of the product. The baseline value taken as a mean of these two values. The product will be consumed immediately after this within 15 minutes and further bloodsamples will be taken at 15, 30, 45, 60, 90 and 120 minutes after starting to eat/drink. | — |
Countries
United Kingdom
Contacts
Oxford Brookes Centre for Nutrition and Health (OxBCNH), Department of Sport, Health Sciences and Social Work, Faculty of Health & Life Sciences, Oxford Brookes University