Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06079294

Impact of Confirmed Autoimmune Encephalitis on Brain Glucose Metabolism: a Prospective FDG PET Study

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-08-22

56

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of FDG PET scans to study brain glucose metabolism in patients with confirmed autoimmune encephalitis. This condition is difficult to diagnose early, which is critical for better neurological outcomes. The study focuses on 56 patients diagnosed based on established criteria from 2016 and 2021, aiming to assess the diagnostic value of FDG PET performed during the acute phase before or shortly after starting immunomodulating treatment. Participants will undergo an initial FDG PET scan at the acute phase, either before immunomodulating treatment begins or within 10 days after starting treatment. A follow-up FDG PET scan will be done three months after treatment initiation to analyze changes over time. This prospective study investigates how FDG PET compares to standard imaging like MRI in detecting autoimmune encephalitis. During the study, participants will have brain FDG PET scans at the specified times, with evaluations of brain glucose metabolism as the main outcome. Researchers will monitor the initial scan results and follow-up scans to understand disease progression and treatment impact. The total study participation involves scans before and three months after treatment, along with assessments to confirm diagnosis and eligibility.

CONDITIONS

Brief Title

Impact of Confirmed Autoimmune Encephalitis on Brain Glucose Metabolism

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Newly diagnosed autoimmune encephalitis based on at least one of the following: definite limbic autoimmune encephalitis per 2016 Graus criteria; possible autoimmune encephalitis with typical autoantibody detected in serum or CSF; probable or certain paraneoplastic neurological syndrome per 2021 criteria (excluding peripheral neurological syndromes)
  • Less than 6 months since first neurological symptoms related to autoimmune encephalitis
  • Affiliated or entitled to a social security system (except AME)
  • Provided free, written, and informed consent (patient, legal representative, or close relative)
Not Eligible

You will not qualify if you...

  • History of brain tumor, head trauma, infarction, or cerebral hematoma likely to alter brain carbohydrate metabolism on PET
  • Immunotherapy for autoimmune encephalitis started more than 10 days ago
  • Pregnant or breastfeeding women
  • Ventilated intubated patients
  • Absolute contraindications to MRI (e.g., pacemaker, cochlear implant)
  • Cognitive disorders preventing cooperation with PET scan
  • Painful or agitated patients unable to remain still in supine position for 30 minutes
  • Persons deprived of liberty or under guardianship or curatorship
  • Participation in other interventional research involving radiopharmaceutical injections

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Within 10 days after screening

Participants undergo an initial brain FDG PET scan performed in the acute phase before immunomodulating treatment or within 10 days of treatment initiation to evaluate brain glucose metabolism.

1 visit (in-person)

Long-term Monitoring

Duration - 3 months after treatment initiation

Participants receive a follow-up brain FDG PET scan approximately 3 months after treatment initiation to assess changes in brain glucose metabolism.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Hospital Pitie Salpetriere

Paris, France, 75013

Actively Recruiting

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Research Team

A

Aurélie Kas, Pr

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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