Efficacy and Safety of an Essential Oil-Based Product System for Immune Support

Running, not enrolling · Not applicable · Has a placebo group

Conditions studied: Healthy

In brief

This randomized, double-blind, placebo-controlled clinical trial will evaluate the safety and efficacy of an essential oil-based product system for immune support in healthy adolescents and adults aged 18-45 years. Participants will be randomized to receive aromatic, topical, internal, or combined use of the investigational product or matching placebo for 30 days. The aromatic intervention consists of overnight diffusion, the topical intervention consists of diluted application to specified areas prior to bedtime, and the internal intervention consists of oral capsule administration twice daily. Study visits will occur at baseline and at the end of the 30-day intervention period. Primary outcomes include changes in immune-related biomarkers, including complete blood count, comprehensive metabolic panel, salivary immunoglobulin A (IgA), and inflammatory cytokines (IL-6, TNF-α, IL-10). Epigenetic markers will also be evaluated. Secondary outcomes include validated subjective assessments of immune status and overall well-being, as well as evaluation of safety and tolerability. The study includes an adaptive design with interim analysis to assess enrollment and study continuation parameters.

Key facts

Study ID

NCT07482644

Run by

dōTERRA International

People needed

40

Starts

2026-06-10

Expected to finish

2026-09-17

Last updated by the study team

2026-07-14

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy male or female participants aged 18 to 45 years
• Able to read, write, and understand English
• Willing and able to attend study visits at the study site
• Willing to comply with study procedures, including daily use of assigned study product for 30 days
• Willing to refrain from use of essential oils (topical, aromatic, or internal) outside of the study during the study period
• If previously using essential oils regularly (defined as more than 3 times per week for 2 or more weeks in the past month), must complete a washout period of at least 1 month prior to enrollment

You may not qualify if…

• Known asthma, chronic obstructive pulmonary disease (COPD), chronic lung disease, heart disease, or other medical condition that would make inhalation of essential oils unsafe, as determined by the investigator
• Known allergy or hypersensitivity to essential oils or components of the placebo preparation
• Current use of tobacco products, including smoking, vaping, or chewing tobacco
• Use of recreational drugs
• Pregnant or breastfeeding, or pregnancy within the past 3 months
• Current regular use of essential oils (defined as more than 3 times per week for 2 or more weeks within the past month) without completion of a 1-month washout period
• Initiation of new botanical supplements during the study period
• Any medical, psychiatric, or social condition that, in the opinion of the investigator, would interfere with safe participation or study compliance

Where it is running

• dōTERRA International — Pleasant Grove, Utah, United States

Full record on ClinicalTrials.gov

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