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Diabetes drug may alter your taste buds and food desires

NCT ID NCT02674893

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
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 looked at how the diabetes medication Liraglutide (Victoza) affects taste, food cravings, and eating habits in people with type 2 diabetes who are overweight. Researchers compared three groups: patients starting Liraglutide, diabetic patients not on the drug, and healthy volunteers. They measured changes in wanting, liking, and salivation in response to food over several months. The study was terminated early, so results are limited.

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

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

48 people

The number who actually took part.

Started

Feb 2014

Finished

Aug 2016

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 years and older

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: DIABETIC PATIENTS TREATED WITH LIRAGLUTIDE * persons who have provided written informed consent * aged \> 18 years * type 2 diabetes with HbA1C \> 7% * overweight (BMI \> 27) * normal renal function (creatinine clearance \> 50ml/min) * patients to be treated with Liraglutide (patients with type 2 diabetes with HbA1C \> 7.5% and overweight or obesity, whose current treatment is insufficient to control the diabetes). CONTROL DIABETIC PATIENTS * persons who have provided written informed consent * aged \> 18 years * type 2 diabetes with HbA1C \> 7% * overweight (BMI \> 27) * patients for whom treatment with Liraglutide is not indicated * normal renal function (creatinine clearance \> 50ml/min) HEALTHY SUBJECTS * persons who have provided written informed consent * aged \> 18 years Exclusion Criteria: DIABETIC PATIENTS TREATED WITH LIRAGLUTIDE * type 1 diabetes * decompensated congestive heart failure * acute or chronic infection, progressive cancer, liver cirrhosis * ongoing treatment with antibiotics * smoking * chronic alcohol abuse (\>4 glasses a day) * aversion to the products to be eaten or smelled * poor understanding of the cognitive tasks requested * treatment interfering with olfactogustatory performance, such as psychotropic, anti-emetic and anti-ulcer drugs * persons without national health insurance cover * persons under guardianship * hypersensitivity to Liraglutide * pregnancy, breastfeeding * history of acute or chronic pancreatitis * calcitonin level at selection ≥ 50 ng/L * liver disease, defined by a level of alanine aminotransferase (ALAT) ≥ 2.5 times the upper limit of normal (ULN) for reference values CONTROL DIABETIC PATIENTS * type 1 diabetes, * decompensated congestive heart failure, * acute or chronic infection, progressive cancer, liver cirrhosis, * ongoing treatment with antibiotics, * smoking * chronic alcohol abuse (\> 4 glasses a day), * aversion to the products to be eaten or smelled, * poor understanding of the cognitive tasks requested, * treatment interfering with olfactogustatory performance, such as psychotropic, anti-emetic and anti-ulcer drugs. * persons without national health insurance cover * persons under guardianship HEALTHY SUBJECTS * diabetes (type I and II) * sensory disorders * decompensated congestive heart failure, * acute or chronic infection, progressive cancer, liver cirrhosis, * ongoing treatment with antibiotics, * smoking * chronic alcohol abuse (\> 4 glasses a day), * aversion to the products to be eaten or smelled, * poor understanding of the cognitive tasks requested, * treatment interfering with olfactogustatory performance (psychotropic, anti-emetic, anti-ulcer drugs) * persons without national health insurance cover * persons under guardianship * contra-indications to MRI, notably, but not limited to: pace maker, implantable cardiac defibrillators, neurostimulators, cochlear implants, certain implanted automated injection systems (insulin pumps), vascular intracerebral ferromagnetic clips, certain systems to regulate intravascular temperature, myopia requiring the patients to wear spectacle, history of stroke or transient ischemic attack (TIA), metallic foreign body, in particular intraocular or situated near high-risk zones (nervous system, vascular system), claustrophobia….

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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.

Contacts and locations

Locations

  • CHU de DIJON

    Dijon, 21079, France

More trials for these conditions

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