Glycaemia Clinical Trial
— GLYCOFOS-creamOfficial title:
Postprandial Glycaemic and Insulinaemic Responses After Consumption of Dairy Desserts Containing Fructo-oligosaccharides in Adults.
The study aims to evaluate the glycaemic and insulinaemic response of short-chain fructo-oligosaccharides (scFOS) used to replace sugars (e.g. dextrose) in foods.
Status | Completed |
Enrollment | 27 |
Est. completion date | February 2014 |
Est. primary completion date | February 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 50 Years |
Eligibility |
Inclusion Criteria: - Body mass index (BMI) between 18.0 and 25.0 kg/m² (included) - Ready to keep the same volume of physical activity and the same dietary habits during the study and particularly 24 hours before each visit - Be used to have breakfast - Non-smoker for at least 3 months - For the female participant: not being pregnant or breastfeeding and using efficient birth control - Signed the consent form - Able to follow the instructions of the study - Health insured - Accepted to be included in the National Registry for biomedical research Volunteers (Fichier VRB, Volontaires Recherches Biomédicales). Exclusion Criteria: - Fasting blood glucose over 6.1 mmol/L (1.10 g/L) (or diabetes treated or not) - Fasting blood cholesterol over 6.35 mmol/L - Fasting blood triglycerides over 1.70 mmol/L (or history of insulinoma) - Fasting blood insulin under 20 mU/L - Fasting HbA1c under 7% - History of hypercholesterolemia, hypertension, diabetes or glucose intolerance treated or not - History of dietary allergies or coeliac disease - History of digestive system disease susceptible to modify digestion or absorption like Crohn's disease - Somatic or psychiatric disorders - Renal insufficiency (kidney failure) - SGOT or ALAT over 52.5 U/L - Smoker - Consuming more than 3 alcoholic beverage a day - Weight varied 3 kg the last 3 months |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science
Country | Name | City | State |
---|---|---|---|
France | NutrInvest - Institut Pasteur de Lille | Lille | Nord |
Lead Sponsor | Collaborator |
---|---|
Institut Pasteur de Lille | Syral |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Glycaemic response | Blood glucose kinetics with 7 points. Analysis of the Area under the curve of glucose. | 2 hours and 5 minutes | No |
Secondary | Insulinaemic response | Blood insulin kinetics with 7 points. Analysis of the Area under the curve of insulin. | 2 hours and 5 minutes | No |
Secondary | Blood glucose peak (Cmax) | Peak of blood glucose during kinetics. | One-time data (the highest one) within the 2hrs 5mins kinetics. | No |
Secondary | Blood insulin peak (Cmax) | Peak of blood insulin during kinetics. | One-time data (the highest one) within the 2hrs 5mins kinetics. | No |
Secondary | Glucose Tmax : time to reach the peak of blood glucose | One time within the 2hrs 5mins kinetics. | No | |
Secondary | Insulin Tmax : time to reach the peak of blood insulin | One time within the 2hrs 5mins kinetics. | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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