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Chewing gum that fights belly fat? new study tests probiotic approach

NCT ID NCT05882149

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a special probiotic chewing gum could help people with abdominal obesity lose belly fat and improve blood sugar control. 124 adults with large waistlines chewed either the probiotic gum or a placebo gum for 12 weeks. Researchers measured changes in waist size, body fat, and other health markers to see if the gum offered any benefits.

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.

Participants

124 people

The number who actually took part.

Started

Jun 2023

Finished

Feb 2025

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 80 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: 1. Male and female subjects ≥ 18 years old. 2. Established diagnosis of abdominal obesity: waist circumference (WC) ≥ 102 cm for men and ≥ 88 cm for women. 3. Voluntary, written, signed, informed consent to participate in the study. 4. Agreement to comply with the protocol and study restrictions. 5. Females of child-bearing potential require to provide a negative urine pregnancy test. Exclusion Criteria: 1. WC \< 102 cm for men, \<88 cm for women, and \>150 cm. 2. BMI ≥ 40 kg/m2. 3. Diagnosed and pharmacologically-treated type 1 or type 2 diabetes (fasting blood glucose ≥ 7 mmol/l). 4. Subjects with serious autoimmune disease, cardiovascular disease, liver dysfunction/disease, kidney dysfunction/disease, dementia, pancreatic disease, history of cancer within past 5 years, anemia, or any other disease or condition which, in the Investigator's opinion, could interfere with the results of the study or the safety of the subject. 5. Immunosuppression or ongoing therapy causing immunosuppression. 6. Pharmacologically-treated (medication/supplements) dyslipidemia. 7. Subjects consuming antibiotics in the previous 1 month. 8. Subjects consuming probiotics and prebiotics at least 1 month prior to inclusion in the study or during the intervention period. 9. Use of drugs or supplements to manage body weight or body fat in the last 3 months. 10. Use of laxatives or fiber supplements in the past 4 weeks. 11. History of chronic active inflammatory disorders. 12. History of bariatric surgery. 13. History of any chronic gastrointestinal disease (e.g. IBD). 14. Regular use of systemic or inhaled corticosteroids, or systemic immunomodulatory drugs. 15. Significant change in tobacco, snuff, nicotine and e-cigarette use habits in the past 3 months or planned cessation of the use of these products during the trial. 16. Active or recent (last 3 months) participation in a weight loss program (diet and/or exercise). 17. Weight change (increase or loss) of 3 kg during the past 3 months. 18. Pregnant or planning pregnancy during the study or breastfeeding. 19. Participation in a clinical trial with an investigational product or drug within 60 days prior to screening. 20. Illicit drug users. 21. Alcohol abusers. 22. Known hypersensitivity to any ingredients in the active or placebo products.

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Conditions

The condition(s) this trial relates to.

Obesity, Abdominal

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Universitat Rovira i Virgili

    Reus, Tarragona, 43201, Spain

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Other studies related to the condition(s) this trial covers.