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NCT Number: NCT06693960

Evaluating the Pharmacokinetics of Oregano and Potential Oregano-drug Interactions Using a Drug Cocktail Approach

The purpose of this clinical trial is to determine how the supplement oregano affects how the body metabolizes pharmaceutical drugs.

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Key information

Conditions

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Washington State University College of Pharmacy and Pharmaceutical Sciences

Spokane, Washington, 99202, United States

Location status: Recruiting

Location contact

John White, PharmD, PA-C

SUB_INVESTIGATOR

Mary F Paine, RPh, PhD

CONTACT

[email protected]

509-358-7759

Mary F Paine, RPh, PhD

PRINCIPAL_INVESTIGATOR

Matthew Layton, MD, PhD

SUB_INVESTIGATOR

About this study

Oregano (Origanum vulgare) is a flowering plant native to Europe. The fresh or dried leaves are commonly used as a cooking herb. Oregano oil extracts are also marketed as herbal supplements. O. vulgare ranked as the number 12 top-selling herbal supplement in the natural channel in 2022. Oregano supplements are consumed for myriad purported medicinal properties, including antimicrobial, antioxidant, and anti-inflammatory effects. Oregano contains multiple types of compounds, including phenols, terpenes, and terpenoids. Recent compelling in vitro data showed that an extract of O. vulgare activated the human pregnane X receptor (PXR) and aryl hydrocarbon receptor (AhR), which regulate the expression and activity of the prominent drug metabolizing enzymes cytochrome P450 (CYP) 3A4 and CYP1A2, respectively. PXR also regulates the expression and activity of several other CYPs (e.g., CYP2C9, CYP2C19), as well as transporters (e.g., the efflux transporter P-glycoprotein (P-gp)). The extent of activation of both receptors by O. vulgare rivaled that of St. John's wort, a well-known herbal supplement that induces CYP and P-gp activity in human participants. These investigators next evaluated the effects of O. vulgare on CYP3A4 and CYP1A2 activity in human hepatocytes. Again, the extent of induction by O. vulgare rivaled that of St. John's wort. Collectively, these observations suggest that oregano supplements could precipitate numerous interactions with pharmaceutical drugs.

The primary objective of the proposed study is to evaluate the potential for a well-characterized O. vulgare product to precipitate pharmacokinetic interactions with a "cocktail" of oral drugs that are substrates for multiple CYPs. The investigators and others have shown this validated cocktail (caffeine, dextromethorphan, losartan, midazolam, and omeprazole) to be safe to administer to healthy adult participants. The secondary objective is to determine the pharmacokinetics of the oregano supplement, which to date have not been rigorously characterized in humans. Results will be used to help inform healthcare practitioners and consumers about the safe use of this increasingly popular herbal supplement when consumed with certain pharmaceutical drugs.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Between 18-64 years old and healthy
  • Not taking any medications (prescription and non-prescription) or dietary/herbal supplements that can interfere with study drug pharmacokinetics
  • Willing to abstain from consuming dietary/herbal supplements and citrus juices for several weeks
  • Willing to abstain from cannabis/marijuana, hemp, and THC- and CBD-containing products for several weeks
  • Willing to abstain from consuming caffeinated beverages or other caffeine-containing products the evening before and the morning of the first day of each study arm
  • Willing to abstain from consuming any alcoholic beverages for at least 1 day prior to any study day and during the study day
  • Willing to use a secondary method of birth control that does not include the introduction or discontinuance of hormonal-based birth control (such as abstinence, copper IUD, or condoms). Specifically, regardless of the use hormonal-based birth control, a non-hormonal method should be used for the duration of the study and for three weeks following cessation of participation.
  • Willing to abstain from consuming oregano (as a food additive or otherwise) for the duration of the study
  • Geographically located within a 40-mile radius of Spokane and have the time to participate

Exclusion criteria

  • Under 18 or over 64 years old
  • Taking medications or dietary/herbal supplements that can interfere with study drug pharmacokinetics
  • Have a major illness
  • Taking medication/supplements for a mineral deficiency
  • History of intolerance or allergy to oregano or any of the cocktail drugs (caffeine, dextromethorphan, losartan, midazolam, and omeprazole)
  • Use of cannabis/marijuana, hemp, and CBD- and/or THC-containing products within the last month
  • Currently using drugs or illicit substances for recreational purposes
  • Pregnant or nursing
  • Geographically located outside the 40-mile radius of Spokane and do not have the time to participate
  • Cannot read and speak English

Treatment and study plan

Oregano

Dietary Supplement

Oil of oregano administered as a softgel (180 mg).

Drug Cocktail

Drug

Oral drug cocktail consisting of caffeine (100 mg), dextromethorphan (30 mg), losartan (25 mg), midazolam syrup (2 mg), and omeprazole (20 mg).

Primary outcomes

  1. Midazolam Area under the plasma concentration vs. time curve (AUC) ratio

    Time frame: 0-24 hours

    Ratio of the area under the plasma concentration vs. time curve of midazolam in the presence to absence of oregano.

Secondary outcomes

  1. Caffeine AUC ratio

    Time frame: 0-24 hours

    Area under the plasma concentration vs. time curve of caffeine in the presence to absence of oregano.

  2. Caffeine maximum plasma concentration (Cmax) ratio

    Time frame: 0-24 hours

    Ratio of the maximum plasma concentration of caffeine in the presence to absence of oregano.

  3. Caffeine half-life ratio

    Time frame: 0-24 hours

    Ratio of the half-life of caffeine in the presence to absence of oregano.

  4. Dextromethorphan AUC ratio

    Time frame: 0-24 hours

    Area under the plasma concentration vs. time curve of dextromethorphan in the presence to absence of oregano.

  5. Dextromethorphan Cmax ratio

    Time frame: 0-24 hours

    Ratio of the maximum plasma concentration of dextromethorphan in the presence to absence of oregano.

  6. Dextromethorphan half-life ratio

    Time frame: 0-24 hours

    Ratio of the half-life of dextromethorphan in the presence to absence of oregano.

  7. Losartan AUC ratio

    Time frame: 0-24 hours

    Ratio of the area under the plasma concentration vs. time curve of losartan in the presence to absence of oregano.

  8. Losartan Cmax ratio

    Time frame: 0-24 hours

    Ratio of the maximum plasma concentration of losartan in the presence to absence of oregano.

  9. Losartan half-life ratio

    Time frame: 0-24 hours

    Ratio of the half-life of losartan in the presence to absence of oregano.

  10. Midazolam Cmax ratio

    Time frame: 0-24 hours

    Ratio of the maximum plasma concentration of midazolam in the presence to absence of oregano.

  11. Midazolam half-life ratio

    Time frame: 0-24 hours

    Ratio of the half-life of midazolam in the presence to absence of oregano.

  12. Omeprazole AUC ratio

    Time frame: 0-24 hours

    Area under the plasma concentration vs. time curve of omeprazole in the presence to absence of oregano.

  13. Omeprazole Cmax ratio

    Time frame: 0-24 hours

    Ratio of the maximum plasma concentration of omeprazole in the presence to absence of oregano.

  14. Omeprazole half-life ratio

    Time frame: 0-24 hours

    Ratio of the half-life of omeprazole in the presence to absence of oregano.

Study contacts

Contact information is provided by the study sponsor or research team.

Mary F Paine, RPh, PhD

CONTACT

[email protected]

509-358-7759

Sponsors and collaborators

Lead sponsor

Washington State University

Other

Collaborators

  • National Center for Complementary and Integrative Health (NCCIH)
  • Office of Dietary Supplements (ODS)

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Nov 19, 2024
Registry last updated
Jun 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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