Data

A double-blinded placebo-controlled parallel design trial to determine whether inhibiting intestinal sweet taste sensing improves glycaemic responses in patients with type 2 diabetes

South Australian Health and Medical Research Institute

Dataset description

Intestinal sweet taste receptors (STRs) sense all sweet stimuli to coordinate the absorption and metabolism of glucose. A defect in intestinal STRs in patients with type 2 diabetes (T2D), as well as supplementation of low-calorie sweeteners in non-diabetic subjects, both accelerate glucose absorption and worsen glycaemic control. This is a double-blinded placebo-controlled parallel design trial to determine whether inhibiting intestinal sweet taste sensing improves glycaemic responses in patients with type 2 diabetes, by blocking intestinal STRs in patients with T2D.

Date Information

Collected from 2021/2024
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Source Study

Trial acronym

Not available

Trial ID

ACTRN12621000981820

Funding

Charities/Societies/Foundations, Diabetes Australia

Scientific enquiries

A/Prof Richard L Young

Brief Summary

Intestinal sweet taste receptors (STRs) sense all sweet stimuli to coordinate the absorption and metabolism of glucose. We have shown that a defect in intestinal STRs in patients with type 2 diabetes (T2D), as well as supplementation of low-calorie sweeteners in non-diabetic subjects, both accelerate glucose absorption and worsen glycaemic control. We now propose to block intestinal STRs in patients with T2D to evaluate the potential glycaemic benefits of this potential 'next generation' diabete .... Read more

Key Inclusion Criteria

i) Volunteers with Type 2 Diabetes Mellitus (American Diabetes Association criteria) managed by metformin alone (morning dose of metformin will be withheld until after study day lunch on each visit, to reduce effects on gut hormone responses) ii) HbA1c less than or equal to 8.5% iii) Body mass index (BMI) 25 - 35 kg/m2 iv) Haemoglobin above the lower limit of the normal range (i.e. above 135g/L for men and above 115g/L for women), and ferritin above the lower limit of normal (above 20ng/mL for w .... Read more

Key Exclusion Criteria

i) Significant illness, other than type 2 diabetes, including impairment to cardiovascular or respiratory function that limits a participant’s activity and represents a risk to safe placement of a nasoenteral catheter. ii) History of gastrointestinal disease, including significant upper gastrointestinal symptoms (assessed by validated gastrointestinal symptom questionnaire), pancreatitis, or previous gastrointestinal surgery (other than uncomplicated appendectomy or cholecystectomy) iii) Impaire .... Read more

Can healthy volunteers participate?

No

Population

Sample Size    40

Min. age    40 Years

Max. age    79 Years

Sex    Both males and females

Condition category    Type 2 Diabetes Mellitus

Condition code    Metabolic and Endocrine

Intervention

Intervention code Treatment: Other

Patients with Type 2 Diabetes Mellitus will be screened then undergo two study day visits in a randomised, double-blinded manner. Study day one will occur prior to diet supplementation, with study day two immediately following four weeks of diet supplementation with placebo capsules or capsules containing the sweet taste blocker, lactisole (300mg). Single capsules will be consumed immediately prior to meals, three times daily. Adherence to intervention will be monitored by capsule return and pat ....
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Comparison

Control group Placebo

Adherence to placebo treatment (microcellulose) will be monitored by capsule return and patient diary.

Outcomes

Outcome: Proportional increase in the incremental area under the curve (iAUC), peak and/or time-to-peak for serum 3-OMG levels (absorption) for lactisole vs. placebo supplementation during intraduodenal glucose infusion
Timepoint: Study visit 1, T = -10, 0, 10, 20, 30, 40, 50, 60, 90 and 120 min (primary timepoint) during (T = 0-30) and post-glucose challenge pre-study, and study visit 2, T = -10, 0, 10, 20, 30, 40, 50, 60, 90 and 120 min (primary timepoint) during (T = 0-30 ....

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Outcome: Proportional increase in the incremental area under the curve (iAUC), peak and/or time-to-peak for blood glucose for lactisole vs. placebo supplementation during intraduodenal glucose infusion
Timepoint: Study visit 1, T = -10, 0, 10, 20, 30, 40, 50, 60, 90 and 120 min (primary timepoint) during (T = 0-30) and post-glucose challenge pre-study, and study visit 2, T = -10, 0, 10, 20, 30, 40, 50, 60, 90 and 120 min (primary timepoint) during (T = 0-30) and post-glucose ....

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The data-sharing statement for this study is currently unavailable.

Source study information is derived from the Australian New Zealand Clinical Trials Registry (ANZCTR). For more information on the ANZCTR, please see anzctr.org.au

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