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Completed

NCT Number: NCT02335008

The Effect of Artificial Sweeteners (AFS) on Sweetness Sensitivity and Preference - Pilot

The goal of this study is to test the hypothesis that repeated consumption of artificial sweetener reduces sweet taste intensity.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The John B Pierce Laboratory

New Haven, Connecticut, 06519, United States

About this study

Significant controversy surrounds the possibility that consumption of artificial sweeteners (AFS) leads to weight gain. Some studies have found correlations between AFS use and weight gain and/or diabetes [1-4] while others have indicated that AFSs may aid in weight loss [5] or have no effects on body mass index (BMI) [6]. In rats, exposure to AFS leads to reduced chow intake following a sweet preload [7, 8], higher body weight [9, 10] and increased glucose responses and decreased GLP1 release following an oral glucose tolerance test [11] compared to exposure to caloric sweeteners. Given that the five FDA approved AFSs are found in thousands of foods [12] this marks a clear and significant gap in knowledge. Our preliminary data demonstrate a 3-fold decrease in sweet taste sensitivity following consumption of a beverage sweetened with two packets of Splenda for just 10 days. These data provide strong evidence that repeated exposure to sucralose reduces perception of sweet taste intensity, most likely by down-regulation of the sweet taste receptor. Therefore, it is imperative that we gain a greater understanding of the consequences of AFS use, since alterations in sweet taste perception that occur in response to AFS exposure may promote weight gain.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy
  • Fluent in English

Exclusion criteria

  • History of oral nerve damage,
  • presence of known taste or smell disorder,
  • food allergies or sensitivities (for example nuts, lactose, artificial sweeteners),
  • history of CNS disease,
  • diabetes,
  • history of DSM-IV major psychiatric disorder, including alcohol and substance abuse, chronic use of medication that may affect taste,
  • conditions that may interfere with gustatory or olfactory perception (colds, seasonal allergies, recent smoking history),
  • aberrant stimulus ratings,
  • contra-indication for fMRI,
  • uncomfortable swallowing in supine position.

Treatment and study plan

Sucralose

Dietary Supplement

2 packets per 12 fl oz

Sucrose

Dietary Supplement

equisweet to sucralose

Primary outcomes

  1. Ratings of taste sensitivity

    Time frame: up to one week after intervention

    general labeled magnitude scale ratings of taste intensity

Sponsors and collaborators

Lead sponsor

Yale University

Other

Registry information

Official study title

The Effect of Artificial Sweeteners (AFS) on Sweetness Sensitivity and Preference - Pilot Study

Acronym: AFS_pilot

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jan 9, 2015
Registry last updated
Jul 15, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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