Clinical Trials Directory

Trials / Completed

CompletedNCT04289454

Sensory Analysis and Taste Modulation of Ketone Esters

Ketone Esters for Optimization of Operator Performance in Hypoxia Technical Volume (Sub-project: Sensory Analysis and Taste Modulation of the Ketone Ester)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
19 (actual)
Sponsor
Monell Chemical Senses Center · Academic / Other
Sex
All
Age
21 Years – 45 Years
Healthy volunteers
Accepted

Summary

Ketone ester (KE) drinks are sold commercially in the USA and elsewhere (the FDA has accepted a GRAS (generally regarded as safe) notification on the KEs we propose to study). KE drinks can have beneficial effects on metabolism. Unfortunately, KE drinks have a strongly unpleasant flavor which can trigger rejection. The current study will generate data to help inform KE drink formulations with improved flavor. First stage, trained subjects will rate the intensity of various sensation qualities (e.g., bitter, sour, metallic, and astringent) from KE drinks to help understand the nature of the unpleasant flavor and the particular sensory systems involved (e.g., taste vs. smell). Then, subjects will taste KE drinks with and without various flavor modifiers. Subjects will be healthy adults (aged 21-45) without known food allergies.

Conditions

Interventions

TypeNameDescription
OTHERFlavor additiveVarious flavor additives will be tested (vs. no added flavor) to determine which show promise for making KE drinks taste less unpleasant

Timeline

Start date
2020-08-30
Primary completion
2021-06-04
Completion
2021-06-04
First posted
2020-02-28
Last updated
2022-03-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04289454. Inclusion in this directory is not an endorsement.