Status:

COMPLETED

Contribution of Inflammation and Neuronal Integrity Markers in Patients With First-episode Conversive Motor Disorder

Lead Sponsor:

Centre Hospitalier Universitaire de Nīmes

Conditions:

Conversion Disorder

Eligibility:

All Genders

18-65 years

Brief Summary

Conversion disorders, also called "dissociative disorders" (ICD-10), or "functional neurological disorders" (DSM-5), are a common condition, with a prevalence of 1-10% in medical and surgical inpatien...

Detailed Description

This project is an ancillary study carried out from the cohort of patients included in the HYCORE protocol "PET-Scan evaluation of metabolic abnormalities associated with the clinical evolution at 6 m...

Eligibility Criteria

Inclusion

  • The patient must have given free and informed consent and signed the consent.
  • Patient must be enrolled in or a beneficiary of a health insurance plan.
  • Patient's age is \> 18 and ≤ 65 years.
  • Patient meets DSM-IV criteria for conversive motor disorder (with paralysis, motor weakness, or abnormal movements) evolving for less than 1 month and is euthymic (HAMD score \< or =7 assessed by a psychiatrist).
  • First episode (incident case)
  • The last symptom is less than one month old.
  • The patient is not on neuroleptics.

Exclusion

  • Subject is participating in another study
  • Subject is in an exclusion period determined by a previous study
  • Subject is under court protection, guardianship, or conservatorship
  • The subject refuses to sign the consent form
  • It is impossible to provide the subject with informed information
  • The patient is pregnant, parturient, or nursing
  • Specialized neurological clinical examination and brain and spinal cord MRI reveal organic neurological damage
  • The subject presents a HAMD score \>7
  • Subject has a current manic or hypomanic episode, a current diagnosis of substance abuse/dependence (excluding tobacco), a lifetime diagnosis of schizophrenia, or a chronic neurological condition (active epilepsy, stroke, brain tumor)
  • Suicidal or high-risk subjects (assessed using the MINI)
  • The subject has a contraindication to the performance of a PET scan
  • Patient is on neuroleptic medication at inclusion
  • The last symptom is more than one month old
  • The patient has already had an episode (prevalent case).

Key Trial Info

Start Date :

April 1 2022

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

April 15 2022

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT05305014

Start Date

April 1 2022

End Date

April 15 2022

Last Update

November 17 2025

Active Locations (1)

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1

Ismael CONEJERO

Nîmes, Choisir Une Région, France, 30029