NL-OMON43100CompletedNot Applicable
Continuous glucose monitoring during diets that differ in glycemic load - GLOW<br>Glucose LOWering
nilever0 sites23 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 23
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 to 64 (—)
Inclusion Criteria
- •- Apparently healthy men and post-menopausal women (post-menopausal for at least one year)
- •- BMI >= 25.0 and <= 35.0 kg/m2
- •- Age: 50-70 yrs
- •- Signed informed consent
Exclusion Criteria
- •- Having a medical conditions which might affect the study measurements.
- •- Reported use of over-the-counter or prescribed medication or food supplements, which may interfere with study measurements.
- •- Use of oral antibiotics 40 days or less prior to the start of the study
- •- Reported participation in another nutritional or biomedical study 3 months before the screening or during the study
- •- Reported participation in night shift work 2 weeks prior to screening or during the study.
- •- Reported intense sporting activities > 2h/w.
- •- Reported alcohol consumption > 10 units/week (female) or > 14 units/week (male)
- •- Reported use of any nicotine containing products in the 6 months preceding the study and willing to abstain from use of nicotine containing products during the study.
- •- Reported dietary habits: medically prescribed diet, slimming diet, vegetarian.
- •- Reported weight loss/gain (> 3 kg) in the last 2 months before the study.
- •- Blood donation in the past 3 months
- •- Known allergy or intolerance to food products.
Investigators
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