Essential Oils for Digestive Health

NS
RO
Overseen ByRussell Osguthorpe
Age: 18 - 65
Sex: Any
Trial Phase: Academic
Sponsor: dōTERRA International

What You Need to Know Before You Apply

What is the purpose of this trial?

This study aims to evaluate the efficacy of specific essential oils. Efficacy will be evaluated through changes, if any, to hsCRP, gene expression, and standard hematologic and metabolic parameters, as well as subjective health changes as measured by Gastrointestinal Symptom Rating Scale (GSRS), PROMIS Global Health survey, PROMIS Fatigue Scale, Immune Fitness Item Scale (IFIS), and the Immune Status Questionnaire (ISQ) in healthy volunteers. The main questions it aims to answer are:

1. Do specific essential oils affect gene expression and hematologic and metabolic parameters as measured in blood?

2. How do essential oils affect gut microbiome?

3. How does daily use of specific essential oils affect subjective quality of life and health parameters?

4. Is ingesting and topically applying specific essential oils daily safe, as measured by laboratory tests and adverse events?

Two study products will be used: oil for topical use, supplement for internal use. The two products will be used together and compared to a placebo group. The topical oil contains a blend of ginger essential oil, peppermint essential oil, caraway essential oil, coriander essential oil, and anise essential oil. The supplement contains everything the oil has, plus anise essential oil.

Participants will:

* Be assigned one of the two groups.

* Use the oil topically once each day for 4 weeks.

* Take one supplement in the morning and one in the evening every day for 4 weeks.

* Attend 2 study visits in which they provide blood and urine (females only) samples.

* Complete 2 stool collection/microbiome kits

* Complete surveys and subjective health assessments

Who Is on the Research Team?

NS

Nicole Stevens

Principal Investigator

doTERRA International LLC

Are You a Good Fit for This Trial?

Inclusion Criteria

Willing and able to use study products as directed daily for about 4 weeks
Willing to avoid alcohol, recreational drugs, tobacco, and vaping for the duration of the study
Willing to track use of study products
See 13 more

Exclusion Criteria

Failure to meet all listed inclusion criteria

What Are the Treatments Tested in This Trial?

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: Dietary supplement and topical oilExperimental Treatment2 Interventions
Group II: PlaceboPlacebo Group2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

dōTERRA International

Lead Sponsor

Trials
7
Recruited
580+