Does the form of a supplement change how well the body absorbs it?
NCT ID NCT07804758
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This study tests whether a liposomal form of the supplement palmitoylethanolamide (PEA) is absorbed into the body better than an ultra-micronized form. Six healthy adults will take a single 600 mg dose of each version, with a week between doses, and give blood samples over 24 hours. Researchers will compare how much PEA reaches the bloodstream and how quickly it is cleared. The goal is to see if the delivery method affects the supplement's availability in the body.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Two oral forms of the dietary supplement palmitoylethanolamide (PEA): an ultra-micronized version and a liposomal version, each given as a single 600 mg dose.
- What this could lead to
- If one form is absorbed better, it could point to a more effective way to deliver PEA supplements.
- What could go wrong
- This is a very small early study in healthy people, so results may not apply to the general public or to people with health conditions.
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
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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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6 people
The number who actually took part.
- Started
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Apr 2026
- Finished
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Apr 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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 70 years
- Sex
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Anyone
- 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: * Aged 18-70 years * BMI 18-30 kg/m² * Healthy participants * Written informed consent Exclusion Criteria: * Use of PEA-based supplements in the preceding 2 weeks. * Significant liver, kidney, gastrointestinal or metabolic conditions. * Known allergy or intolerance to PEA or excipients. * Pregnancy or breastfeeding
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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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Crabion S.R.L.
Corciano, PG, 06073, Italy
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