Grape extract gummies vs capsules: which delivers more health-boosting flavanols?
NCT ID NCT06665958
First seen Jul 01, 2026 · Last updated Jul 02, 2026 · Updated 1 time
Summary
This study compares how well flavanols from grape seed extract are absorbed by the body when taken as a capsule or a gummy. Twenty-five healthy men aged 18–40 will each try both forms in a random order. The goal is to see which form leads to higher levels of flavanols in the blood, which could guide the development of better supplements and functional foods.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- grape seed extract (polyphenols)
- What this could lead to
- If successful, this could help develop better dietary supplements or functional foods that deliver more effective polyphenol health benefits.
- What could go wrong
- This is a small, early-stage study in healthy young men, so results may not apply to the general population or translate into real health effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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
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25 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Sep 2025
- Lead sponsor
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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
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18 to 40 years
- Sex
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Male participants only
- Healthy volunteers
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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: * Males * Aged 18-40 years at recruitment * BMI ≥ 20 and \< 30kg/m2 * Considered healthy based on their medical history and physical examination. * Subjects capable of and willing to comply with the protocol and to give their written informed consent. Exclusion Criteria: * Existing chronic disease including any; cardiovascular, neurological, gastric/intestinal, hepatic/pancreatic, renal or hematological diseases, obstructive cardiomyopathy, myocardial infarction, intracranial hypertension, diabetes mellitus (type I or II), chronic kidney disease, clinically significant arrhythmia, metabolic anomaly, ischaemia heart disease. * Uncontrolled Hypertension (\>160/100 mm Hg) or hypotension (\<100/60mm Hg) * Current use of any medication or narcotics within 2 weeks prior to study entry. * Currently on a clinically prescribed diet regimen. * Self-reported alcohol intake of \>10 units/ week * Have taken antibiotic therapy within the last 3 months * Following any specific diet (vegetarian, vegan, etc.) * Consumption of dietary supplement(s) currently or within 4 weeks prior to study entry (i.e. botanicals, vitamins, minerals, amino acids). * Weight change \> 10% of total body weight within the 6 months before entry to study. * Any intolerance or allergy documented or suspected to one of the components of the study products. * Having a psychological or linguistic inability to sign the informed consent; Under legal protection (guardianship, wardship) or deprived from his rights following administrative or judicial decision; * Subject participating in another biomedical study or participation in another study within the 3 months before entry into this study.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ulster University,Human Intervention Studies UnitColeraine, Co. Londonderry BT521SA
Coleraine, Co. Londonderry, BT52 1SA, United Kingdom
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