CClinicalTrials.gg
CompletedNCT00978900Updated Sep 17, 2009

Effects of Artificial Sweetener on Gastrointestinal (GI) Peptide Secretion

A Phase 1 interventional study of Artificial sweeteners; Carbohydrate Sugars and Water in Healthy, sponsored by University Hospital, Basel, Switzerland. Completed. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2009-09-17.

Sponsored by University Hospital, Basel, Switzerland · Phase 1, Interventional, and Basic science

Phase
Phase 1
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

The purpose of this study is to examine the influence of artificial sweeteners (aspartame, acesulfame K, sucralose) and carbohydrate sugars (glucose, fructose) on the release of gastrointestinal satiety hormones in humans.

Read the detailed description

Artificial Sweeteners significantly lower energy density of foods and beverages. They are used by diabetics as sugar substitutes as well as by consumers as aids for dietary control. Despite numerous studies which show mainly no influence of artificial sweeteners on glucose metabolism and food intake, discrepancies consist about the real effects of artificial sweeteners. Studies by Blundell and Hill in 1986 have however shown that the consumption of artificial sweeteners resulted in an increase of appetite ratings; the efficiency of AS has therefore been questioned. With respect to the world wide increase in the prevalence in obesity, it seems important to clarify whether artificial sweeteners can help regulate body weight or not. This study will explore the effect of artificial sweeteners on the release of the gastrointestinal satiety hormones PYY, GLP-1, GIP and ghrelin.

02

Conditions studied

  • Healthy

Keywords

  • satiety peptides
  • GLP-1
  • PYY
  • ghrelin
  • appetite profile
  • Sweetening Agents
03

In context

Lead sponsor

University Hospital, Basel, Switzerland is the lead sponsor of 968 studies on the registry; 191 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy subject with a body-mass index of 19.0-24.5
  • Normal eating habits
  • Age 18-40 years
  • Stable body weight for at least three months

Exclusion criteria

Exclusion Criteria:

  • Smoking
  • Substance abuse
  • Regular intake of medications (except for oral contraceptives)
  • Medical or psychiatric illness
  • history of gastrointestinal disorders
  • food allergies
05

Study design

Phase
Phase 1
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
12 participants (actual)

Study arms

  • Active comparator
    Acesulfame K

    Dietary Supplement: Artificial sweeteners; Carbohydrate Sugars

  • Active comparator
    Sucralose

    Dietary Supplement: Artificial sweeteners; Carbohydrate Sugars

  • Active comparator
    Aspartame

    Dietary Supplement: Artificial sweeteners; Carbohydrate Sugars

  • Active comparator
    Glucose

    Dietary Supplement: Artificial sweeteners; Carbohydrate Sugars

  • Active comparator
    Fructose

    Dietary Supplement: Artificial sweeteners; Carbohydrate Sugars

  • Placebo comparator
    Water

    Dietary Supplement: Water

Interventions

  • Dietary supplementArtificial sweeteners; Carbohydrate Sugars

    sweetening agent dissolved in tap water, administered via intragastric tube

  • Dietary supplementWater
06

What researchers measure

Primary outcomes

  1. Gastrointestinal peptide secretion

    Time frame: 2 hour blood sampling

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 17, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00978900
Lead sponsor
University Hospital, Basel, Switzerland
First posted
Sep 17, 2009
Start date
Dec 2008
Primary completion
Mar 2009
Completion
Jul 2009
Last update
Sep 17, 2009

Study contacts

Christoph Beglinger, MD
principal investigator · Clinical Research Center, University Hospital Basel

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2009. You cannot join it, but the record below documents what was studied.

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