Chewing gum for weight loss? study pulled before it started
NCT ID NCT07045766
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study planned to test a fiber-enriched chewing gum (FibreGum) as a way to help with weight management in healthy adults with a BMI between 23 and 40. The goal was to see if people would actually use the gum and find it acceptable, not to measure weight loss directly. However, the study was withdrawn before any participants were enrolled, so no data was collected.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- FibreGum chewing gum (galactooligosaccharides)
- What this could lead to
- If it had worked, this could have pointed toward a simple, accessible way to support healthy weight management using a fiber-enriched gum.
- What could go wrong
- The study was withdrawn before enrolling anyone, so no results are available. The approach was only being tested for feasibility, not effectiveness, and any weight loss would likely be modest.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Started
-
Jan 2026
- Finished
-
Apr 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Written Informed Consent * Healthy adults aged 18 to 65 years (inclusive), as determined by the investigator * BMI of 23 to 40 kg/m2 (inclusive) * Living in Switzerland * Ability and willingness to follow the study protocol (e.g., cognitive capacity for compliance, gum chewing) * Access and willingness to use an electronic device (e.g., mobile phone, computer or tablet) * Access to a scale to self-report weight Exclusion Criteria: * Current weight loss therapy with Glucagon-like Peptide 1 (GLP-1) agonists or other non-prescription products (at investigator's discretion) * Treatment with a GLP-1 agonist within the past 2 months * Initiation/Discontinuation of nicotine product use (\>1 nicotine product per day, e.g., (e-)cigarette, gum) within the last 2 months (at investigator's discretion) * Significant change in medication within the last 2 months (at investigator's discretion) * Unable to chew gum 3 times daily (e.g. due to dental issues, at investigator's discretion)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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