Clinical Trials Directory

Trials / Completed

CompletedNCT02999321

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
93 (actual)
Sponsor
Purdue University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

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

Detailed description

Participants will be randomly assigned to one of three parallel arms: 0% (water), 5 mg, 15mg aspartame. Participants will have an oral glucose tolerance test at the beginning and end of a 12 week intervention. . Participants will report to the lab weekly for 12 weeks to pick up their next week's intervention products and measurements for body weight, waist circumference, blood pressure and heart rate. They will consume their intervention products daily for 12 weeks. They will record appetite sensations and collect a 24 hour urine sample at weeks 0, 4, 8, and 12.

Conditions

Interventions

TypeNameDescription
OTHERaspartamewill be given 5mg aspartame or 15 mg aspartame
OTHERwatercontrol group

Timeline

Start date
2016-08-17
Primary completion
2017-05-05
Completion
2017-05-05
First posted
2016-12-21
Last updated
2018-01-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02999321. Inclusion in this directory is not an endorsement.