Exploration of Glutamatergic System With PET Radiotracer in Gilles de la Tourette Patients: Pilot Study (GlutaTour)

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Recruiting
CT.gov ID
NCT03681795
Collaborator
(none)
24
1
2
48.2
0.5

Study Details

Study Description

Brief Summary

Gilles de la Tourette syndrome is a neuropsychiatric disorder characterized by motor and vocal tics often associated with psychiatric comorbidities (obsessive compulsive disorder, anxiety and depressive syndrome, impulsivity). The pathophysiology of Gilles de la Tourette syndrome remains unclear.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Experimental MRI exam and PET scan exam with radiotracer
N/A

Detailed Description

Gilles de la Tourette syndrome is a neuropsychiatric disorder characterized by motor and vocal tics often associated with psychiatric comorbidities (obsessive compulsive disorder, anxiety and depressive syndrome, impulsivity). The pathophysiology of Gilles de la Tourette syndrome remains unclear. It would involve an alteration of striatal-cortico-thalamic cortical circuits resulting in dopaminergic dysfunction. But glutamatergic hypothesis is also discussed from pharmacological, biochemical and genetic arguments. Exploration of glutamatergic system can be done in humans in vivo using a new radiotracer: the [18F] FNM (Fluoroethylnormemantine), a derivative of memantine. In the present study, aim of the study

  1. to show the glutamatergic system "in vivo" in patients with Tourette's syndrome and 2) to perform correlations between various motor and behavioral symptoms and the pattern of brain fixation for this radiotracer. To do that, a pilot study will be conducted in 12 patients with Tourette's who will be evaluated in terms of motor (tics) and behavioral (OCD, anxiety, depression, impulsivity) symptoms. Each patient will have a PET-scan exam and a brain MRI exam. Data analysis will be carried out from two different approaches: first by region of interest, and secondly, without topographic a priori with the Statistical Parametric Mapping (SPM) software.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
compare PET-evaluated glutamaergic system activity ([18F]-FNM) between patients with Gilles de la Tourette and healthy volunteers paired in sex, age and manual lateralitycompare PET-evaluated glutamaergic system activity ([18F]-FNM) between patients with Gilles de la Tourette and healthy volunteers paired in sex, age and manual laterality
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Exploration of Glutamatergic System With PET Radiotracer in Gilles de la Tourette Patients: Pilot Study (GlutaTour)
Actual Study Start Date :
Nov 26, 2018
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: patient

patients with Gilles de la Tourette syndrome

Diagnostic Test: Experimental MRI exam and PET scan exam with radiotracer
MRI exam and PET scan exam with radiotracer

Experimental: Control

healthy control

Diagnostic Test: Experimental MRI exam and PET scan exam with radiotracer
MRI exam and PET scan exam with radiotracer

Outcome Measures

Primary Outcome Measures

  1. Correlation coefficients [Day 1]

    Correlation coefficients is determined between the fixation of the PET tracer and the Total Tic score (TTS - from 0 to 50) which reflects the severity of tics in patients (under the Yale Global Tic Severity Scale - YGTSS)(Leckman and al, 1989).

Secondary Outcome Measures

  1. Yale Global Tic Severity Scale (YGTSS) [Day 1]

    This scale represents the severity of tics in patients, it is a scale composed of three subscales: Motor tic severity from 0 to 25, Vocal Tic severity from 0 to 25, Overall Impairment from 0 to 50, which reflects the functional impairment score (under Yale Global Tic Severity Scale - YGTSS). This score assesses the repercussions of the syndrome on self-esteem, and the social, professional and family. For each of the sub-scales, tics are rated according to their number, frequency, intensity, complexity, interference with activities of everyday life. The sum of Motor Tic severity and Vocal Tic severity form the Total Tic score (0 to 50)

  2. Yale Brown Obsessive Compulsive Scale (Y-BOCS) - II de 0 à 80) [Day 1]

    Yale Brown Obsessive Compulsive Scale consists of 19 questions aimed at evaluating the severity, the impact on daily, social, family and professional life activities of OCD, the anxieties generated by OCD Higher values represent a worse outcome

  3. Hospital Anxiety Depression [Day 1]

    Hospital Anxiety Depression (from 0 to 42) which is a self-questionnaire of 14 items: 7 items refer to anxiety, 7 items refer to depression. Each item is scored from 0 to 3 This scale explores anxiety and depressive symptoms. Total the anxiety and depression side: maximum 21 points for each. Between 8 and 10: doubtful anxiety or depressive state. Beyond 10: certain anxiety or depression.

  4. Barrat Impulsivity Scale 11 [Day 1]

    Barrat Impulsivity Scale 11 is self-assessment scale with 34 items. It provides an assessment of impulsivity according to motor impulsivity, cognitive impulsivity and planning difficulty. Each item is scored on 4, the total score therefore varies from 0 to 120

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Gilles de la Tourette syndrome according to the American Psychiatric association criteria (5 th ed, American Psychiatric association (APA), 2013)

  • Aged 18 and over

  • Patients treated with 2nd-generation neuroleptics for at least 3months

  • Signed consent form

Exclusion Criteria:
  • contraindications for MRI exam

  • claustrophobia

  • person under exclusive period for another study

  • pregnant women

  • patients under non-authorized treatment (1rst generation neuroleptics) or non-treated by neuroleptics

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital Pierre-Paul Riquet - CHU Toulouse Toulouse France 31059

Sponsors and Collaborators

  • University Hospital, Toulouse

Investigators

  • Principal Investigator: Christine BREFEL-COURBON, MD, University Hospital, Toulouse

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Toulouse
ClinicalTrials.gov Identifier:
NCT03681795
Other Study ID Numbers:
  • 15 7836 03
  • 2017-000816-40
First Posted:
Sep 24, 2018
Last Update Posted:
Sep 1, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Toulouse
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 1, 2021