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Cephalic Phase Responses to Nutritive and Non-Nutritive Sweeteners

NCT06387316 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-04-29

No results posted yet for this study

Summary

This study will focus on changes in blood sugar in response to tasting different types of sweeteners using continuous glucose monitoring (CGM) technology.

Conditions

  • Pre Diabetes

Interventions

OTHER

No Oral Stimulation

No oral stimulation

OTHER

Oral water stimulation

Oral water stimulation

OTHER

Oral Salt Stimulation

Oral Salt Stimulation

OTHER

Oral Sucralose Stimulation

Oral Sucralose Stimulation

OTHER

Oral Sucrose stimulation

Oral Sucrose stimulation

Sponsors & Collaborators

  • Purdue University

    lead OTHER

Principal Investigators

  • Richard Mattes, PhD · Purdue University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2024-03-26
Primary Completion
2024-04-17
Completion
2025-03-30

Countries

  • United States

Study Locations

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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 NCT06387316 on ClinicalTrials.gov