Diabetes drug may alter your taste buds and food desires
NCT ID NCT02674893
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.
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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
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Feb 2014
- Finished
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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
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: 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
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CHU de DIJON
Dijon, 21079, France
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Other studies related to the condition(s) this trial covers.
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