Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07110207

Single-centre Descriptive Study of Taste in Frontotemporal Lobar Degeneration Through the Analysis of Taste Evoked Potentials

Led by Centre Hospitalier Universitaire Dijon · Updated on 2025-08-24

20

Participants Needed

1

Research Sites

101 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The FRONTAL-PEG study focuses on taste perception in frontotemporal lobar degeneration (FTLD). This neurodegenerative disease, characterised by progressive loss of nerve cells, is the second leading cause of dementia after Alzheimer's disease. Patients with FTLD often experience olfactory disorders (= sense of smell) and eating disorders: increased appetite, increased food intake and excessive consumption of sugary foods and snacking. This often leads to excessive weight gain. These eating disorders are still poorly understood at present. In this context, we hypothesise that an alteration in the gustatory pathway - i.e. the way in which the brain perceives taste - could contribute to the eating disorders frequently observed in frontotemporal dementia (FTD), particularly in the marked attraction to sweet foods. We therefore wish to objectively evaluate the taste response to a sweet solution (sucrose) in patients with FTLD, using taste evoked potentials (TEPs). Taste evoked potentials are a reliable and reproducible technique for assessing brain activity in response to taste stimulation. One of their advantages is that they are non-invasive. This study will document, for the first time in this disease, the characteristics of cortical (brain) processing of taste information. The FRONTAL-PEG study is an interventional, regional, single-centre study conducted at the Dijon University Hospital, in collaboration with the CMRR (Memory, Resources and Research Centre) and the CSGA (Centre for Taste and Food Sciences). All investigations are carried out at the CSGA (building adjacent to the Dijon University Hospital), with the exception of blood tests, which are carried out at the Dijon University Hospital. The total duration of participation in the study is one morning. No follow-up is planned at the end of the study.

CONDITIONS

Official Title

Single-centre Descriptive Study of Taste in Frontotemporal Lobar Degeneration Through the Analysis of Taste Evoked Potentials

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Person who has given their free and informed consent
  • Person of legal age
  • Fasting more than 2 hours before PEG measurement
  • Body Mass Index (BMI) less than 30 kg/m² (according to medical record data)
  • Diagnostic criteria for established or probable frontotemporal lobar degeneration (DLFT)
Not Eligible

You will not qualify if you...

  • Not affiliated with or not covered by a social security scheme
  • Subject to legal protection measures (guardianship, trusteeship)
  • Subject to judicial protection measures
  • Pregnant women, women in labour, or breastfeeding women
  • MMSE score less than 15 and/or MoCA score less than 10
  • Known COVID-19 infection within 6 months prior to inclusion
  • Active smokers (more than 4 cigarettes per day regularly)
  • Subject with a pacemaker (contraindicated for bioelectrical impedance analysis)
  • Subject with diabetes (type 1 or type 2)
  • Taking medication during the study that interferes with taste

AI-Screening

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Trial Site Locations

Total: 1 location

1

CHU Dijon Bourgogne

Dijon, France

Actively Recruiting

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Research Team

A

Agnès JACQUIN-PIQUES

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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