Essential oil pills: do capsules change how they work?
NCT ID NCT07581522
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how healthy adults absorb frankincense, lemon, and wild orange essential oils when taken in different types of capsules. Nineteen people took part, and researchers measured oil levels in the blood over 24 hours. The goal was to see if the capsule type changes how fast or how much oil gets into the body, and to check for any safety concerns.
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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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19 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Dec 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 35 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.
Selection Criteria: Participants must meet all the following criteria: * Adults ages 18-35 years old * Local to metropolitan Jackson, MS, and/or willing to come to the clinical research center for study visits * Willing to wash out of all internally consumed essential oil and botanical products for at least 2 weeks prior to starting the study and willing to maintain the washout for the duration of the study (approximately 8 weeks) * Willing to avoid all frankincense, wild orange, and lemon essential oil in any form (aromatic, topical, or internal) for the duration of the study (approximately 5 weeks). * Willing to avoid alcohol, recreational drugs, and smoking/vaping for 3 days prior to each arm of the study * Willing to receive an intravenous catheter in the arm or hand every two weeks for 4 weeks (three times total) * History of successful blood/plasma donation, IV insertion, or blood collection by phlebotomy * Weigh at least 110 pounds * No uncontrolled metabolic disease * No unstable major diseases under treatment by healthcare professional * No pregnancy within the last 60 days or currently breastfeeding (females) * No allergy to olive oil or frankincense, lemon, or wild orange essential oils * No regular internal consumption of frankincense, lemon, or wild orange essential oil regularly within the last 1 month (regularly is defined as dosing daily for more than 2 consecutive weeks, or dosing more than 2-3 times per week for 4 consecutive weeks) * No alcohol, recreational drug, or smoking/vaping use in the past 3 days * No evidence of medical condition, significant disease or disorder, medication, or surgery within the past 12 months that may, in the judgment of the medical provider, put the participant at risk or affect study results, procedures, or outcomes * Not currently or previously participating in any other clinical trial within the last 30 calendar days
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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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University of Mississippi Medical Center
Jackson, Mississippi, 39216, United States
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