NCT07110207 · RECRUITING

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

This study looks at how the brain responds to a sweet taste in people with frontotemporal lobar degeneration, a different dementia from Alzheimer's. Researchers use a painless scalp recording of brain activity while participants taste a sugar solution. It is a one-morning observational-style study, not a test of any drug, so there is no phase.

You may qualify if

  • Person who has given their free and informed consent
  • Person of legal age
  • Fasting > 2 hours before PEG measurement
  • Body Mass Index (BMI) \< 30 kg/m² (according to medical record data)
  • DLFT: diagnostic criteria for established or probable DLFT

You're excluded if

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

The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.

Eligibility criteria as of 2025-08-24

View full record on ClinicalTrials.gov

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