Clinical Utility of Handheld Hydrogen Breathalyzer in Identification of Food Sensitivities (AIRE Study)

NACompletedINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

October 1, 2020

Primary Completion Date

March 10, 2025

Study Completion Date

March 20, 2025

Conditions
SIBOSmall Bowel Bacterial Overgrowth Syndrome
Interventions
DEVICE

Hydrogen content recording

Eligible participants will eat participants' normal, typical diets during the first week of the study. Participants will use the AIRE machine to measure exhaled H2 content before and after two meals each day - the first meal of the day and the last meal of the day. Participants will breathe into the AIRE machine before eating to obtain a baseline value. Once participants have finished eating, participants will breathe into the AIRE machine 30 minutes, 60 minutes, and 90 minutes postprandially. The participants will record participants' food intake and symptoms directly into participants' smartphone via an app that comes with the AIRE device.

Trial Locations (1)

21224

Johns Hopkins Bayview Medical Center, Baltimore

All Listed Sponsors
collaborator

FoodMarble

UNKNOWN

lead

Johns Hopkins University

OTHER

NCT04309396 - Clinical Utility of Handheld Hydrogen Breathalyzer in Identification of Food Sensitivities (AIRE Study) | Biotech Hunter | Biotech Hunter