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D-allulose, a low-calorie sugar, provides an attractive alternative to sucrose and added sugars in products. This study aimed to verify the tolerance of d-allulose in children, in doses that are Generally Recognised As Safe (GRAS) and below maximum tolerable levels on g/kg basis.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Allulose Dose 1 | Active Comparator | Fruit-flavoured drink with allulose at Dose 1 (2.5 g per 120 ml) |
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| Allulose Dose 2 | Active Comparator | Fruit-flavoured drink with allulose at Dose 2 (4.3 g per 120 ml) |
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| Placebo Comparator: Control (CON) | Placebo Comparator | Control drink containing high fructose corn syrup. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| D-allulose | Dietary Supplement | Fruit-flavoured drink with d-allulose at 2 dosages |
|
| Measure | Description | Time Frame |
|---|---|---|
| Difference in the number of participants experiencing at least one stool that met a Type 6 or Type 7 description on the Bristol Stool Chart, within 24 hours after study product intake | Difference in the number of subjects experiencing at least one stool that met a Type 6 or Type 7 description on the Bristol Stool Chart | within 24 hours after study product intake |
| Measure | Description | Time Frame |
|---|---|---|
| Number of subjects who experienced at least one loose or watery stool that met a Type 6 or Type 7 description on the Bristol Stool Chart | Stool frequency, measured as the number of subjects who experienced at least one loose or watery stool that met a Type 6 or Type 7 description on the Bristol Stool Chart | in a 24-hour period post-consumption of intervention |
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Inclusion Criteria:
Exclusion Criteria:
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Acute, randomised, double-blind, placebo-controlled, cross-over
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| Placebo | Dietary Supplement | Fruit-flavoured drink with high fructose corn syrup |
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| Frequency of the GI symptom event and frequency of participants reporting GI symptoms events by the severity and causality (i.e., related, not related) for each treatment group recorded at Visits 3, 5 and 7, for pre- and post-dose administration | Report common gastrointestinal symptoms including abdominal pain, bloating, cramping, abdominal rumbling, excess flatus, and and nausea associated with d-allulose consumption. These were reported as the frequency of the event and frequency of participants reporting events by the severity and causality (i.e., related, not related) for each treatment group recorded at Visits 3, 5 and 7, for pre- and post-dose administration. The severity of the event was categorized in three levels (mild, moderate, severe). | in the 24-hour period post-consumption |