Buckwheat drink may tame blood sugar spikes after meals
NCT ID NCT03923205
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
Researchers at the University of Aberdeen are testing whether a buckwheat beverage can reduce blood sugar spikes after meals. The study includes healthy adults and people with type 2 diabetes whose condition is managed by diet or metformin. Participants drink the beverage and have their blood sugar and insulin levels measured over five hours. The goal is to see if buckwheat's natural compounds can help control post-meal glucose, which is important for preventing diabetes complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a buckwheat beverage
- What this could lead to
- If it works, this could point toward a natural dietary drink that helps people with type 2 diabetes manage blood sugar after meals, potentially reducing complications.
- What could go wrong
- This is a small early study with only 28 participants, so results may not apply widely. The effect on blood sugar may be modest, and the beverage is not a replacement for diabetes medication.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
28 people
The number who actually took part.
- Started
-
Mar 2019
- Finished
-
Mar 2022
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Healthy and T2D (controlled by diet and lifestyle or metformin) volunteers; Age 18+; males and females. Exclusion Criteria: For the healthy group: * taking prescribed medication * HbA1c above 48mmol/mol (or 6.5%) * pregnant or breastfeeding * blood donation in the last three months * unable to give written informed consent * eating disorders such as anorexia, bulimia, binge eating or night eating syndrome. * significant health issue * taking vitamin or mineral supplements (unless they agree to discontinue supplementation 2 weeks or more before the start of the study) * Food allergies/intolerances For the T2D groups: * T2D controlled by medication other than metformin * pregnant or breastfeeding * blood donation in the last three months * unable to give written informed consent * eating disorders such as anorexia, bulimia, binge eating or night eating syndrome. * any other significant health issue other than T2D * taking vitamin or mineral supplements (unless they agree to discontinue supplementation 2 weeks before the start of the study) * food allergies/intolerances
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Rowett Institute, University of Aberdeen
Aberdeen, AB 25 2ZD, United Kingdom
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