CClinicalTrials.gg
Status unknownNCT04614506Updated Mar 22, 2022

Transcranial Magnetic Stimulation to Measure Cortical Excitability in Dravet Syndrome

An observational study in Dravet Syndrome, sponsored by Boston Children's Hospital. Status unknown at 1 site in United States. Open to participants aged 6 Months to 30 Years. Per ClinicalTrials.gov, last updated 2022-03-22.

Sponsored by Boston Children's Hospital · Observational

The sponsor has not verified this record recently (last verified Mar 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
6
Ages
6 Months to 30 Years
Sex
All
01

Study summary

Dravet syndrome (DS) is an epileptic encephalopathy caused by pathogenic variants in the SCN1A gene resulting in medically refractory epilepsy and psychomotor delays.

As a pilot study assessing for feasibility, the investigators aim to test whether alterations in cortical excitatory:inhibitory ratio can be reliably recorded. The investigators will utilize transcranial magnetic stimulation (TMS) metrics of cortical excitatory and inhibitory tone as an initial step towards translating findings from rodent genetic models of DS into disease-specific biomarkers and offer future measures of therapeutic target engagement in this patient population.

Participants will complete two visits, each consisting of a TMS session and an EEG session. Visits will be scheduled 4-8 weeks apart.

Read the detailed description

This is a single site study to be conducted at Boston Children's Hospital (BCH) investigating the neurophysiological biomarkers of epilepsy and developmental disability in children and young adults with Dravet Syndrome.

Mechanistically, the features of the DS phenotype are attributable to a loss of cortical inhibition. TMS is a non-invasive form of focal cortical stimulation in which an external powerful magnet induces an electrical field intracranially over the stimulated region that is used to interrogate or modulate states of cortical excitation or inhibition.

Accordingly, the investigators propose to test whether metrics of cortical excitability and inhibition can be obtained by transcranial magnetic stimulation (TMS) and EEG in patients with DS.

02

Conditions studied

  • Dravet Syndrome
03

In context

Epilepsies, Myoclonic

87 studies on the registry are indexed under Epilepsies, Myoclonic; 23 are open to participants now.

This study's planned enrollment of 6 is below the median of 90 across 19 observational studies indexed under Epilepsies, Myoclonic.

Browse Epilepsies, Myoclonic studies →

Lead sponsor

Boston Children's Hospital is the lead sponsor of 598 studies on the registry; 151 are open to participants now.

Of its 31 completed or terminated interventional studies of FDA-regulated products, 18 (58%) have results posted.

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

04

Who can participate

Ages eligible
6 Months to 30 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Children and adults diagnosed with Dravet Syndrome.

Inclusion criteria

  • Age: 6 months - 30 years
  • Ability to obtain informed consent with the participant or legally authorized representative
  • DS confirmed by pathogenic variant in SCN1A gene
  • Medical history consistent with clinical phenotype of DS

Exclusion criteria

Exclusion Criteria:

  • Comorbid conditions such as a second genetic diagnosis which may confound interpretation.
  • Current or planned participation in a clinical drug or device trial.
  • Previous participation in a gene therapy or gene editing trial
  • Allergy to adhesives used for surface EMG electrodes
  • Contraindications to TMS (e.g. implanted devices for which there is no TMS safety data)
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
6 participants (estimated)
Patient registry
No

Groups and cohorts

  • Subject with DS

    Participants will complete two visits spaced out by 4 - 8 weeks to undergo neurophysiological assessments (Electroencephalogram \[EEG\], and Transcranial magnetic stimulation \[TMS\]).

    Device: Transcranial Magnetic Stimulation (TMS) · Device: Electroencephalogram (EEG)

Interventions

  • DeviceTranscranial Magnetic Stimulation (TMS)

    Transcranial magnetic stimulation (TMS) is a method for noninvasive electrical cortical stimulation, where small intracranial currents are generated by a powerful, fluctuating, extracranial magnetic field. TMS is unique in its capacity for experimental, diagnostic, and therapeutic utility. Single pulse (spTMS) and paired-pulse TMS (ppTMS) have been used extensively to study, measure, and modulate cortical excitability and plasticity.

    Also known as: Nexstim Navigated Brain Stimulation (NBS) System 4

  • DeviceElectroencephalogram (EEG)

    These will be an ambulatory EEG recordings that span 24 hours and done without sedation. Recordings will be performed using electrode locations specified by the international 10-20 system for standard clinical practice.

    Also known as: Natus

06

What researchers measure

Primary outcomes

  1. Resting motor threshold (% machine output)

    Resting motor threshold (rMT) is obtained by single-pulse TMS and measures voltage-gated sodium-channel-mediated cortical excitability. It is the minimum intensity of stimulation needed to reliably evoke a motor evoked potential (MEP) of at least 50 microvolts in over 50% of trials. It is reported as a percentage of total machine output.

    Time frame: 1 year

  2. Durations of cortical silent period (ms)

    Cortical Silent Period (CSP) is a single-pulse TMS measure of GABA-mediated cortical inhibition, in which stimulation is applied to the motor cortex while subjects are activating a target muscle (here, abductor pollicis brevis and deltoid muscles), resulting in a pause in muscle contraction. The time between stimulation and the return of voluntary muscle activity is the CSP, measured in milliseconds (ms).

    Time frame: 1 year

  3. Ratio of motor evoked potential amplitudes (no units)

    Facilitation (ICF) are paired-pulse TMS metrics of cortical inhibition and excitability, respectively. A short interval interstimulus (1-5 ms) leads to cortical inhibition reflective of GABAergic neurotransmission; a longer interval interstimulus of 10-20 ms leads to a cortical facilitation, which reflects glutamatergic neurotransmission; an even longer interstimulus interval of 50-300 ms reflects GABAB-mediated local inhibition and likely GABAA-mediated network inhibition. The ratio of the peak-to-peak amplitude (in mm) of the second MEP to the first (or control) MEP will be calculated for each of these stimulation protocols.

    Time frame: 1 year

  4. Cortical Inhibitory Tone

    Power in the gamma (30-80 Hz) frequency band.

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • Boston Children's Hospital
    Boston, Massachusetts 02115, United States
    • Paul MacMullin · Contact · Paul.MacMullin@childrens.harvard.edu
    • Alexander Rotenberg, MD, PHD · Principal investigator
    • Melissa Tsuboyama, MD · Sub investigator
    • Ann Poduri, MD · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04614506
Lead sponsor
Boston Children's Hospital
Collaborators
Encoded Therapeutics
Responsible party
Alexander Rotenberg (Associate, Department of Neurology; Director, Neuromodulation Program; Associate Professor of Neurology, Harvard Medical School, Boston Children's Hospital) — Principal investigator
First posted
Nov 4, 2020
Start date
Nov 2, 2020
Primary completion
Dec 2022 (estimated)
Completion
Dec 2022 (estimated)
Last update
Mar 22, 2022

Study contacts

Paul MacMullin
Contact
Paul.MacMullin@childrens.harvard.edu
617-355-4875
Melissa Tsuboyama, MD
Contact
Melissa.Tsuboyama@childrens.harvard.edu
Alexander Rotenberg, MD, PhD
principal investigator · Boston Children's Hospital

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 status unknown, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion