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CompletedNCT06463093ATEPDIPSYUpdated Jun 25, 2026

Differential Diagnosis of Cognitive Disorders of Psychiatric or Neurodegenerative Origin

An observational study in Neurocognitive Disorders, sponsored by Central Hospital, Nancy, France. Completed at 1 site in France. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-06-25.

Sponsored by Central Hospital, Nancy, France · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
20
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The aim of the research is to analyze whether 18F-FDG PET helps in the diagnosis and therefore in the management of the patient.

Read the detailed description

Neurocognitive disorder or Mild Cognitive Impairment corresponds to a decline in one or more cognitive functions; compared to the previous level of performance.

Indeed, the prevalence of neurodegenerative pathologies is estimated at more than one million according to Santé Publique France, due to the aging of the population. To be compared with the prevalence of the population suffering from a psychiatric disorder estimated at one in five people, or 13 million French people, in 2021.

With the increase in the prevalence of these two entities and their clinical entanglement, the question arises of the origin of neurocognitive disorders, is it a manifestation of a psychiatric pathology or a neurodegenerative pathology not yet diagnosed.

If this is the case, the patient's prognosis is modified with a pejorative evolution and a loss of autonomy which is to be anticipated. This delay deprives the patient and his family of interventions likely to alleviate behavioral disorders; maintain a level of autonomy compatible with life at home; alleviates the burden and improves the quality of life of caregivers.

02

Conditions studied

  • Neurocognitive Disorders
03

In context

Neurocognitive Disorders

246 studies on the registry are indexed under Neurocognitive Disorders; 88 are open to participants now.

This study's enrollment of 20 is below the median of 165 across 93 observational studies indexed under Neurocognitive Disorders.

Browse Neurocognitive Disorders studies →

Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 778 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients treated for psychiatric reasons with neurocognitive disorders in the clinic, having consulted or being hospitalized at the psychotherapeutic center of Nancy between 01/01/2021 to 01/01/2024 and having undergone a flurodeoxyglucose positron emission tomography marked with fluorine 18 carried out in the course of care

Inclusion criteria

  • Adult patients with cognitive impairment
  • Positron emission tomography with flurodeoxyglucose labeled with fluorine 18 carried out in the course of care

Exclusion criteria

Exclusion Criteria:

  • Patients objecting to the collection of their data
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
20 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Neuro cognitive disorders and disorders of neurodegenerative origin in psychiatric population

    Change of the diagnosis before the PET and after the PET

    Time frame: one day

07

Study locations

1 site
  • Nancy's hospital
    Vandœuvre-lès-Nancy, 54511, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06463093
Lead sponsor
Central Hospital, Nancy, France
Responsible party
Antoine VERGER (Principal Investigator, Central Hospital, Nancy, France) — Principal investigator
First posted
Jun 17, 2024
Start date
Nov 30, 2024
Primary completion
Jan 30, 2025
Completion
Jul 2, 2025
Last update
Jun 25, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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