The Effects of Aspartame on Appetite, Body Composition and Oral Glucose Tolerance

NCT02999321 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 93

Last updated 2018-01-18

No results posted yet for this study

Summary

Assess the impact of chronic use of aspartame on glycemia, appetite and body composition.

Conditions

  • Oral Glucose Tolerance

Interventions

OTHER

aspartame

will be given 5mg aspartame or 15 mg aspartame

OTHER

water

control group

Sponsors & Collaborators

  • Ajinomoto USA, INC.

    collaborator INDUSTRY
  • Purdue University

    lead OTHER

Principal Investigators

  • Richard D Mattes, PhD · Purdue University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-08-17
Primary Completion
2017-05-05
Completion
2017-05-05

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 NCT02999321 on ClinicalTrials.gov