Kratom-Oxycodone interaction under the microscope
NCT ID NCT05846451
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether kratom, a plant-based product, changes how the body breaks down and responds to the opioid drug oxycodone. Sixteen healthy adults will take kratom tea, an oxycodone tablet, or both, and researchers will measure drug levels and effects like pupil size. The goal is to understand potential interactions, not to treat any disease.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 16 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- 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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21 to 45 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: * Males and females, aged from 21-45 years and healthy * Body weight between 130 and 250 pounds (60-115 kg) and body mass index between 19 and 30 * Not taking any medications (prescription and non-prescription) or dietary supplements/botanical products known to alter the pharmacokinetics of either oxycodone or kratom * Willing to abstain from consuming dietary supplements/botanical products and fruit juices for several weeks * Willing to abstain from cannabis/marijuana, hemp, and THC- and/or CBD-containing products for several weeks * Willing to abstain from consuming caffeinated beverages or other caffeine-containing products the evening before and morning of any inpatient visit * Willing to abstain from consuming alcoholic beverages for one day prior to any inpatient visit * Willing to use an additional method of contraception that does not include oral contraceptive pills, patches, or other hormonal methods (such as abstinence, copper IUD, or condoms) * Have consumed kratom previously and tolerated it well without any unpleasant effects * Willing to abstain from kratom for several weeks * Have consumed any opioid previously and tolerated it well without any unpleasant effects or addiction * Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for the subject to comply with the requirements of the study * Geographically located within a 40-mile radius of Spokane and have the time to participate Exclusion Criteria: * Males and females under the age of 21 or over the age of 45 * People who weigh less than 130 pounds or more than 250 pounds * People with a body mass index less than 19 or greater than 30 * Any current major illness or chronic illness including but not limited to kidney disease, hepatic disease, diabetes mellitus, hypertension, coronary artery disease, chronic obstructive pulmonary disease, cancer, or HIV/AIDS * No previous exposure to kratom * No previous exposure to an opioid * History of anemia or any other significant hematologic disorder * History of substance abuse, dependence, or addiction or major psychiatric illness * A need for chronic opioid analgesics * Use of opioid analgesics 3 weeks prior to initiation of the study * An imminent likely need for opioid analgesics (e.g., planned dental or surgical procedure) * Pregnant or nursing * History of allergy or intolerance to kratom, other opioids, or oxycodone * Taking concomitant medications, both prescription and non-prescription (including dietary supplements/botanical products), known to alter the pharmacokinetics of kratom or oxycodone * Presence of a condition or abnormality that, in the opinion of the Investigator, would compromise the safety of the patient or the quality of the data * History of sleep apnea * Any prior use of amphetamines, benzodiazepines, cocaine, MDMA, opioids, PCP, or other drugs for recreational purposes * Use of cannabis/marijuana, hemp, THC-containing products, CBD-containing products, or CBD within the last month * Out-of-range clinical laboratory value that the study physician considers participation in the study a health risk * Inability to speak, read, and understand English
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Washington State University College of Pharmacy and Pharmaceutical Sciences
RECRUITINGSpokane, Washington, 99202, United States
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