Comparison of Microbiome Changes in Healthy Adults Following Ketone Ester Consumption

NCT06954675 | Recruiting

• 1 other identifier: 25-43835
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this observational study is to learn if a ketone ester can improve the content of the gut microbiome. The main questions it aims to answer are:

• Does a ketone ester reduce age-related signatures in the gut microbiome?
• What changes occur in the gut microbiome after consuming a ketone ester? Participants will:
• Take a ketone ester every day for seven (7) days
• Collect and ship stool samples within seven (7) days before, during, and within seven (7) days after the study period
• Measure their ketone levels with a urine strip every day after having the drink
• Answer questions about their typical diet on a normal day
• Record their symptoms, if any arise

Conditions

Microbiome Analysis

Keywords

Microbiome; Exogenous ketone; Ketone ester

Outcome Measures

Primary Outcomes (1)

• Longitudinal Change in Microbiome Composition

  Microbiome composition will be defined as the following components: 1) alpha-diversity as calculated by Shannon Index; 2) beta-diversity; and 3) microbial community taxa and gene number.

  From baseline sampling to final sampling, including intervention period, at 21 days

Secondary Outcomes (1)

• Acute Tolerability Symptoms related to Product Ingestion

  From start to end of intervention at 7 days

Study Arms (1)

25g Bis-octanoyl-(R)-1,3-butanediol (C8)

EXPERIMENTAL

Participants will receive 25g of the ketone ester bis-octanoyl-(R)-1,3-butanediol (C8) daily.

Dietary Supplement: Exogenous ketone ester

Interventions

Exogenous ketone ester DIETARY_SUPPLEMENT

25g Bis-octanoyl-(R)-1,3-butanediol (C8)

25g Bis-octanoyl-(R)-1,3-butanediol (C8)

Eligibility Criteria

• Age: 18 Years - 40 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Subject is male or female, 18 to 40 years of age, inclusive, at Virtual Visit 1.
• Subject has a self-reported BMI of 18.5 to 39.9 kg/m2 (inclusive) at Virtual Visit 1.
• Subject is willing and able to comply with all study procedures including maintenance of habitual dietary intake, consumption of study product at specified intervals, written questionnaires including study log and beverage tolerability questionnaire (KETQ), habitual exercise and medication and supplement use.
• Subject has an email address and internet access via computer, phone, or other device, and is willing and able to maintain internet access throughout the trial to complete virtual visits via video conference.
• Subject has no health conditions that would prevent them from fulfilling the study requirements as judged by the Study Clinician on the basis of medical history.
• Subject understands the study procedures and signs forms providing informed consent to participate in the study.

You may not qualify if:

• Subject is unable to converse in English or Spanish
• Subject is unable to provide informed consent due to cognitive impairment or insufficient English or Spanish language comprehension
• Subject has been hospitalized within 30 days of Virtual Visit 1.
• Subject has a clinically important gastrointestinal condition that would potentially interfere with the evaluation of the study beverage \[e.g., inflammatory bowel disease, irritable bowel syndrome, chronic constipation, severe constipation (in the opinion of the Study Clinician), history of frequent diarrhea, history of surgery for weight loss, gastroparesis, systemic disease that might affect gut motility according to the Study Clinician, reflux requiring daily medication, history of gastrointestinal ulcers or bleeding, celiac disease, and/or clinically important lactose intolerance\].
• Subject has a known allergy, intolerance, or sensitivity to any of the ingredients in the study product, including milk protein.
• Subject is undergoing treatment or active surveillance for cancer, or has been diagnosed with cancer in the prior two years, except for non-melanoma skin cancer.
• Subject has recently used antibiotics within 60 days of Virtual Visit 1.
• Subject has extreme dietary habits (e.g., intermittent fasting or time restricted eating, Atkins diet, vegan, very high protein/low carbohydrate or has used weight-loss medications (including over-the-counter medications and/or supplements) or programs within 30 days of Virtual Visit 1.
• Subject has used medications (over-the-counter or prescription) known to influence gastrointestinal function including, but not limited to, opioids, weight loss medications, antidiarrheals, and antispasmodics) within 30 days of Virtual Visit 1.
• Subject has used ketone supplements (ketone salts or esters, and medium chain triglycerides \[MCT\]) within 30 days of Virtual Visit 1.
• Subject is a female who is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential and is unwilling to commit to the use of a medically approved form of contraception throughout the study period. The method of contraception must be recorded.
• Subject has a condition the Study Clinician believes would interfere with their ability to provide informed consent, comply with the study protocol, which might confound the interpretation of the study results, or put the subject at undue risk.

Sponsors & Collaborators

• University of California, San Francisco: lead

Study Sites (1)

UCSF Wayne and Gladys Valley Center for Vision

San Francisco, California, 94158, United States

RECRUITING

Study Officials

• John C Newman, MD, PhD

  University of California, San Francisco

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Sidharth S Madhavan, PhD

CONTACT

248-797-1025; sidharth.madhavan@ucsf.edu

John C Newman, MD, PhD

CONTACT

415-502-5134; Newman@ucsf.edu

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: BASIC SCIENCE
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 11, 2025
• First Posted: May 1, 2025
• Study Start: November 21, 2025
• Primary Completion (Estimated): September 30, 2026
• Study Completion (Estimated): September 30, 2026
• Last Updated: January 26, 2026

Record last verified: 2026-01

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)