Characterization of a Portable Solid-State Breath Acetone Testing Device for Real-Time Ketosis Status

Sponsor
Readout, Inc. (Industry)
Overall Status
Completed
CT.gov ID
NCT04130724
Collaborator
(none)
21
1
1.5
14.2

Study Details

Study Description

Brief Summary

The primary purpose of this study is to characterize the performance and utility of a novel breath acetone meter developed by Readout, Inc.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Blood ketone testing
  • Diagnostic Test: Breath ketone testing

Study Design

Study Type:
Observational
Actual Enrollment :
21 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Characterization of a Portable Solid-State Breath Acetone Testing Device for Real-Time Ketosis Status and Comparison to Blood Ketone Testing
Actual Study Start Date :
Oct 16, 2019
Actual Primary Completion Date :
Nov 30, 2019
Actual Study Completion Date :
Nov 30, 2019

Arms and Interventions

Arm Intervention/Treatment
Ketogenic diet

Subjects consuming either a ketogenic (<30g carbohydrate per day) or a low-carb (<100g carbohydrate per day) diet.

Diagnostic Test: Blood ketone testing
Ketone testing will be done using a blood beta-hydroxybutyrate (BHB) test at least five (5) times per day.
Other Names:
  • Blood ketone testing using the Abbott Precision Xtra meter.
  • Diagnostic Test: Breath ketone testing
    Ketone testing will be done using a breath acetone (BrAce) test at least five (5) times per day.
    Other Names:
  • Breath ketone testing using the Readout breath acetone device.
  • High-carbohydrate diet

    Subjects consuming a high carbohydrate (>100g carbohydrate per day) diet.

    Diagnostic Test: Blood ketone testing
    Ketone testing will be done using a blood beta-hydroxybutyrate (BHB) test at least five (5) times per day.
    Other Names:
  • Blood ketone testing using the Abbott Precision Xtra meter.
  • Diagnostic Test: Breath ketone testing
    Ketone testing will be done using a breath acetone (BrAce) test at least five (5) times per day.
    Other Names:
  • Breath ketone testing using the Readout breath acetone device.
  • Outcome Measures

    Primary Outcome Measures

    1. Correlation between breath acetone (BrAce) and blood beta-hydroxybutyrate (BHB) concentrations [2 weeks]

      Blood BHB and BrAce measurements will be taken simultaneously during at least five (5) measurement sessions each day. After aggregating data from all study participants, the correlation between these two measurements will be determined using regression analysis.

    Secondary Outcome Measures

    1. Reliability of the Readout breath acetone device [2 weeks]

      Multiple BrAce measurements will be taken during each measurement session using the Readout BrAce device and repeatability will be analyzed using alpha reliability coefficients.

    Other Outcome Measures

    1. Utility of a single ketone measurement compared to multiple measurements throughout the day [2 weeks]

      The utility of a single BrAce measurement compared to multiple measurements throughout the day will be assessed by comparing a single measurement for a given user with the time-weighted average of all measurements taken that same day. The probability that a single measurement differs from the time-weighted average of all measurements during the same day will be computed for various difference thresholds.

    2. Time dynamics of breath acetone compared to blood beta-hydroxybutyrate [2 weeks]

      The time dynamics of blood BHB versus BrAce will be explored by performing a correlation calculation between the two measurement methods for various time shifts.

    3. Full-day ketone exposure as measured by breath acetone and blood beta-hydroxybutyrate [2 weeks]

      The full-day ketone exposure as measured by BrAce will be compared with the full-day ketone exposure as measured by blood BHB (12 AM on day 1 to 12 AM on day 2) by first performing linear interpolation between data points on a given day and then calculating the daily area under the curve (AUC) for BrAce and blood BHB. The correlation between blood and breath AUC will be determined by performing regression analysis.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Ketogenic diet cohort: currently following a ketogenic or low-carbohydrate diet defined as less than 30 grams per day (ketogenic) or less than 100 grams per day (low-carbohydrate) as estimated by the individual. Subjects must have been following the diet before the beginning of the study period and must continue with the diet throughout the duration of the trial.

    • High-carbohydrate diet cohort: currently following a diet that does not restrict dietary carbohydrate. Carbohydrate consumption should be greater than 100 grams per day as estimated by the individual. Subjects must have been following the diet before the study period and must continue with the diet throughout the duration of the trial.

    Exclusion Criteria:
    • Type-1 diabetes

    • Insulin-dependent type-2 diabetes

    • History of diabetic ketoacidosis

    • Currently taking Warfarin or other blood thinners

    • Currently taking a sodium-glucose cotransporter-2 (SGLT2) inhibitor

    • Currently taking Disulfiram

    • Unwilling to maintain their diet during the study period

    • Unwilling to test blood and breath ketones five times per day

    • Non-English speaking

    • Persons who are unable or unwilling to follow the study protocol or who, for any reason, the research team considers not an appropriate candidate for this study, including non-compliance with screening appointments or study visits.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Center for Emerging Technologies Saint Louis Missouri United States 63108

    Sponsors and Collaborators

    • Readout, Inc.

    Investigators

    • Principal Investigator: James McCarter, MD, PhD, Readout, Inc.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Readout, Inc.
    ClinicalTrials.gov Identifier:
    NCT04130724
    Other Study ID Numbers:
    • RO-0001
    First Posted:
    Oct 17, 2019
    Last Update Posted:
    Dec 17, 2019
    Last Verified:
    Dec 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 17, 2019