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Enrolling by Invitation

NCT Number: NCT07375329

Breath Hydrogen and Methane as Biomarkers of Fiber Intake

This study is designed to examine if mobile phone-based breath hydrogen and methane monitors can be used as a biomarker of dietary fiber intake.

Enrolling by Invitation

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Key information

Conditions

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Oklahoma Health Sciences

Oklahoma City, Oklahoma, 73104, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be enrolled in parent trial (NCT07219706)

Exclusion criteria

  • Not enrolled in parent trial (NCT07219706)

Treatment and study plan

Breath Tester

Other

Participants enrolled in a fiber-focused study will be offered a Food Marble to see if the data provided correlates with self-reported fiber intake

Primary outcomes

  1. Breath methane

    Time frame: Measured daily for three months

    Measured daily for three months, represented in parts per million (ppm)

  2. Breath hydrogen

    Time frame: Daily for three months

    Measured daily for three months, represented in parts per million (ppm)

Sponsors and collaborators

Lead sponsor

University of Oklahoma

Other

Registry information

Official study title

Exploring the Utility of Breath Hydrogen and Methane as Biomarkers of Total Dietary Fiber Intake: A Pilot Study

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 29, 2026
Registry last updated
Apr 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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