Clinical Trials Directory

Trials / Completed

CompletedNCT01407939

Efficacy of Bitter Blockers on Taste Perception in Children and Adults

Efficacy of Bitter Taste Blockers on Flavor Acceptance in Pediatric Populations

Status
Completed
Phase
Study type
Observational
Enrollment
215 (actual)
Sponsor
Monell Chemical Senses Center · Academic / Other
Sex
All
Age
3 Years
Healthy volunteers
Accepted

Summary

This proposal describes 2 basic research studies that will be conducted sequentially. Study 1 will test the efficacy of both classic and newly developed "generally recognized as a safe" (GRAS) bitter blockers on the perceived bitterness and acceptance of different classes of bitter-tasting compounds by children and compare their responses to adults. Because variations among and between children and adults in terms of sensitivity to different bitter compounds are due in part to genetically determined receptor variation, the investigators will consider genotype when assessing how well bitter blockers perform. In Study 2, the investigators aim to evaluate different methods (forced-choice procedures, hedonic face scales) used for testing children to determine their reliability and reproducibility.

Conditions

Timeline

Start date
2011-04-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2011-08-02
Last updated
2016-03-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01407939. Inclusion in this directory is not an endorsement.