Status:

UNKNOWN

EEG and TMS-based Biomarkers of ALS, MS and FTD

Lead Sponsor:

University of Dublin, Trinity College

Collaborating Sponsors:

Motor Neurone Disease Association, UK

Irish Research Council, IE

Conditions:

Amyotrophic Lateral Sclerosis

Frontotemporal Dementia

Eligibility:

All Genders

18+ years

Brief Summary

The purpose of this observational study is to improve understanding of the biology of why ALS, MS and FTD have different effects on different people and facilitate better measurement of the disease in...

Detailed Description

The aim of this project is to characterize spatiotemporal patterns of central nervous system dysfunction that correlate with clinical features of ALS, MS and FTD, to provide non-invasive electrophysio...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Age \>18 years and able to give informed written or verbal (in the presence of two witnesses) consent.
  • In the case of non-control subjects, a clinical diagnosis of:
  • (i) Probable frontotemporal dementia (FTD) including behavioural variant FTD, semantic dementia or primary progressive aphasia) with supportive brain imaging or known FTD causing genetic mutation (ii) Multiple sclerosis (MS) according to the McDonald criteria (Polman et al., 2011) or (iii) Possible, probable or definite amyotrophic lateral sclerosis (ALS) according to the El Escorial Criteria Revised (Brooks et al. 2000)
  • Exclusion criteria:
  • Any diagnosed neurological/muscular disease other than ALS, MS or FTD
  • Use of neuro- or myo-modulatory medications except riluzole
  • Inability to participate due to disease-related motor symptoms (e.g. inability to sit for the required time or click the mouse to respond)
  • Upper body metallic implants
  • History of seizure disorders in the participant or immediate family members
  • Anxiety-induced fainting
  • Regular migraine
  • Evidence of significant respiratory insufficiency
  • Sleep time \>2 hours below normal and/or alcohol consumption the night before data collection (in which case, recording session will be rescheduled).

Exclusion

    Key Trial Info

    Start Date :

    September 1 2012

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    April 1 2023

    Estimated Enrollment :

    400 Patients enrolled

    Trial Details

    Trial ID

    NCT04918251

    Start Date

    September 1 2012

    End Date

    April 1 2023

    Last Update

    June 8 2021

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    Academic Unit of Neurology, Trinity College Dublin, The University of Dublin

    Dublin, Leinster, Ireland, Dublin 2