Accuracy of Current Techniques in Quantifying Ketone Levels

NCT ID: NCT06909331

Last Updated: 2025-04-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-01-15

Study Completion Date

2019-12-15

Brief Summary

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The purpose of this study is to determine the accuracy of current measuring techniques used to detect physiological ketone levels.

Detailed Description

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Conditions

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Placebo - Control Exogenous Ketone Salt

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Placebo drink

They were provided a placebo drink that was color, calorie and flavor-matched to the experimental drink.

Group Type PLACEBO_COMPARATOR

Placebo drink solution

Intervention Type DIETARY_SUPPLEMENT

Participants consumed a placebo drink that was flavor, color and calorie matched to the experimental drink.

Experimental supplement

They were provided an ketone salt drink.

Group Type EXPERIMENTAL

Exogenous ketone salt

Intervention Type DIETARY_SUPPLEMENT

Exogenous ketone salt supplement will be taken once to determine acute circulating levels of beta-hydroxybuyrate and acetoacetate compared to a control supplement.

Interventions

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Exogenous ketone salt

Exogenous ketone salt supplement will be taken once to determine acute circulating levels of beta-hydroxybuyrate and acetoacetate compared to a control supplement.

Intervention Type DIETARY_SUPPLEMENT

Placebo drink solution

Participants consumed a placebo drink that was flavor, color and calorie matched to the experimental drink.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* 18-35 years

Exclusion Criteria

* taking medications that affect blood pressure, insulin, or renal function, having meta-bolic syndrome factors such as type 2 diabetes, being pregnant, and/or indicating a pre-existing health condition on the health history questionnaire
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Augusta University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Augusta University

Augusta, Georgia, United States

Site Status

Countries

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United States

Other Identifiers

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IRBnet: 1317538

Identifier Type: -

Identifier Source: org_study_id

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