Salivary Interactions With Chemosensations

NCT03883880 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2023-05-25

No results posted yet for this study

Summary

A counterbalanced, crossover design will be used to evaluate whether exposure to flavors vs. a control over time alters the perception of the flavor by changing an individual's salivary protein profile. Participants will complete 3 acute tasting protocols (baseline, after intervention 1, after intervention 2). The interventions will be with the flavor (epigallocatechin gallate, linolenic acid, capsaicin) or a control, in counterbalanced order, and will involve swishing and swallowing a solution of that sample 5 times per day for two weeks. Each of these flavors will be a separate sub-study.

Conditions

  • Diet, Food Choice, Taste

Interventions

OTHER

Epigallocatechin gallate

Colored solution prepared with epigallocatechin gallate to be consumed daily for two weeks during the epigallocatechin gallate intervention.

OTHER

Epigallocatechin gallate control

Colored control solution to be consumed daily for two weeks during the epigallocatechin gallate intervention.

OTHER

Linoleic acid

Colored emulsion prepared with linoleic acid to be consumed daily for two weeks during the linoleic acid intervention.

OTHER

Linoleic acid control

Colored control solution to be consumed daily for two weeks during the linoleic acid intervention.

OTHER

Capsaicin solution

Colored solution prepared with capsaicin to be consumed daily for two weeks during the capsaicin intervention.

OTHER

Capsaicin control

Colored control solution to be consumed daily for two weeks during the capsaicin intervention.

Sponsors & Collaborators

  • National Institutes of Health (NIH)

    collaborator NIH
  • Purdue University

    lead OTHER

Principal Investigators

  • Cordelia Running, PhD · Purdue University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-05
Primary Completion
2019-09-24
Completion
2021-12-01

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03883880 on ClinicalTrials.gov