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Multiple SclerosisNCT04997343

Neurophysiological Assessment in Patients With Multiple Sclerosis

A study testing Neurophysiological assessment and clinical assessment in people with Multiple Sclerosis and Demyelinating Disease, run by University of Roma La Sapienza.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Main aim of this study will be the evaluation of the neurophysiological techniques of Transcranial Magnetic Stimulation (TMS) via electroencephalography (EEG) co-registration (TMS-EEG) with the study of TEPs (TEP: transcranial evoked potentials) as surrogates of white matter and grey matter functional integrity in… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Neurophysiological assessment and clinical assessment
Could I receive a placebo?
No, everyone receives an active treatment
How many people
128 participants
Where
No sites listed yet
Study dates
Oct 2021to 1 Sep 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • MS diagnosis according to the latest McDonald criteria

Who cannot join

  • other neurological or immunological diseases
  • clinical relapses in the 30 days prior to the clinical and neurophysiological evaluation;
  • presence of conditions that contraindicate the execution of Transcranial Magnetic Stimulation (TMS) methods (history of epilepsy, pacemaker, recent head injury).

Trial locations and contacts

No sites are listed yet.

Antonella Conte, MD, PhD contact

00393466584811

antonella.conte@uniroma1.it

About this study

Official title: Neurophysiological Estimates of Cortical Grey and White Matters Damage in Patients With Multiple Sclerosis

Main aim of this study will be the evaluation of the neurophysiological techniques of Transcranial Magnetic Stimulation (TMS) via electroencephalography (EEG) co-registration (TMS-EEG) with the study of TEPs (TEP: transcranial evoked potentials) as surrogates of white matter and grey matter functional integrity in patients with Multiple Sclerosis (MS). Data will be compared with those obtained from a group of healthy control subjects. Secondary aim will be the longitudinal evaluation of these neurophysiological parameters in MS patients during routine clinical and radiological evaluations, performed according to clinical practice, for 12 months.

To this aim a longitudinal multicenter study will be carried out, interventional (for neurophysiological techniques) and observational (for clinical and radiological evaluations), which involves the enrollment of 64 patients diagnosed with MS. Patients will keep their usual therapeutic regimen and their usual clinical-radiological checks according to clinical practice. The control group will consist of 64 healthy subjects, enrolled with prior written informed consent, age and sex-matched with MS patients and selected among the caregivers of the patients. Healthy subjects will only undergo neurophysiological assessment at baseline.

The neurophysiological evaluation will include the study of the propagation of potentials induced by stimulation. This method allows the study of cortical responses in terms of time domain and frequency, obtaining a measurement of interhemispheric connectivity and of microstructural and functional integrity of white matter. In the same way, these methods allow the assessment of grey matter integrity through the study of intracortical excitability.

Read the detailed description

Multiple sclerosis (MS) is a demyelinating disease of the central nervous system (CNS) whose pathogenesis involved both demyelinating events and neurodegeneration. It is on of the most frequent cause of disability in young adults. It is characterized by different clinical phenotypes: currently, the relapsing-remitting form (RR), the most common, and the progressive forms of MS (primary progressive -PP, secondary progressive -SP) are recognized. The relapsing-remitting form is characterized by the presence of acute/subacute onset of clinical events, the appearance of new lesions on magnetic resonance imaging (MRI), or the uptake of gadolinium by a new or pre-existing lesion. The progressive forms, on the other hand, present with a slow accumulation of disability from the onset (PP-MS), or following a relapsing-remitting trend (SP-MS). The clinical scale mainly used for evaluating patients with MS is the Expanded Disability Status Scale (EDSS). Currently, there are several treatments available for the control of the disease and the identification of the correct therapeutic choice can lead to an important slowdown, up to stabilization, of the clinical course of the disease. It is therefore essential, given the existence of different therapeutic strategies, to recognize early those patients who respond in a sub-optimal manner to therapy. To date, the evaluation of the effectiveness of the treatment is based on clinical and radiological data. Several studies have tried to identify new markers of disability, but none of these have entered the routine clinical use. In this context, the possible role of neurophysiology in early identify markers of inflammatory/ degenerative disease activity is outlined.

Among the neurophysiological methods potentially able to identify the inflammatory or neurodegenerative phase of the disease, the most promising results were obtained with transcranial magnetic stimulation (TMS) and electroencephalography (EEG). These methods, already widely used in the clinical setting, are characterized by being reproducible, non-invasive and low-cost. Thanks to the development of EEG systems compatible with magnetic stimulation, it is possible to study the cortical potentials evoked by TMS (TEPs). The TEPs constitute a sensitive and reproducible experimental index of intracortical excitability and allow the identification of specific alterations of different neurological conditions. The study of TEPs offers a better performance than that obtainable using the single techniques, TMS and EEG, separately.

Neurophysiological estimates of white matter integrity Several evidence have confirmed that the EEG indices of functional connectivity are influenced by the degree of myelination of the white matter. Among these indices of EEG connectivity, cortico-cortical coherence is a linear correlation index between the oscillatory signal of two cortical areas and has been shown to be a sensitive index of the myelination state of the brain in physiological conditions and in various neurological pathologies.

Distinct EEG oscillations in the different frequency bands revealed many robust relationships to behavioral, cognitive, and clinical states in several studies. Spatial-temporal oscillatory dynamic patterns recorded by EEG are important brain state-dependent measures of neocortical dynamics, including functional connectivity. Myelin is critical for sustaining oscillatory neural activity and entrainment between "generators" (e.g., cell assemblies or networks at multiple scales) in brain regions separated by substantial conduction delays. Functional connectivity as assessed by scalp EEG at large scales is believed to be strongly influenced by white matter tracts, especially the cortico-cortical projections. The standard Fourier transform-based multi-channel signal measure coherence is a squared correlation coefficient expressed as a function of frequency; it can provide robust measures of cognitive state and white matter (WM) maturation or disease. WM integrity determines propagation delays (i.e. the timing) of synaptic inputs in a determined brain network thus allowing phase synchrony of local oscillations. Relatively small changes in conduction delays can have significant effects on oscillatory coupling and phase synchrony between distant brain regions. Disruption in brain synchronization contributes to dysfunction in many neurological and psychiatric disorders. Compared to scalp EEG, high-resolution EEG (HR-EEG) methods employ computer algorithms (e.g., Laplacian or dura image) to provide estimates of brain or dural surface potentials at roughly the 2-3 cm scale. HR-EEG functional connectivity measures, like narrow band (e.g., 1 Hz) alpha and theta coherence, has been linked to cortico-cortical signal propagation via (mostly) myelinated axons. The propagation time between hemispheres is about 30 ms through myelinated callosal fibers and 150-300ms through unmyelinated fibers. An investigation of scalp-registered inter-hemispheric coherence between the left and right sensorimotor hand areas using HR-EEG revealed a superposition of both bilaterally coherent and incoherent rhythmic activities within the alpha band. Synaptic integration can be expected to be strongly influenced by the degree of myelination of intercallosal axons. Combined EEG and HR-EEG can provide complementary functional connectivity estimates that are maximally sensitive to large/global (~5-10 cm) and intermediate/local {-2-3 cm) spatial scale source regions, respectively. White matter integrity is important for cortico-cortical connections and is critical to these functional connectivity estimates, especially scalp oscillatory coupling and distant sources phase coherence.

Transcranial magnetic stimulation (TMS) is a non-invasive brain-stimulation technique. By producing high-intensity magnetic pulse, TMS induces brief electric currents that can excite or inhibit a small area of the cerebral cortex. This activating property is classically used on the primary motor cortex (M1) to produce action potentials along the cortico-spinal bundle and evoke a motor potential (MEP, motor evoked potential) in the contralateral musculature. In MS patients, EEG and TMS are widely used as diagnostic tools to prove demyelination by means of abnormal conduction time along white matter tracts, even in subjects with normal MRI scans. Furthermore, when the magnetic stimulus is delivered during voluntary muscle contraction of the stimulation target muscle, the TMS of M1 can generate a brief interruption of voluntary electromyography (EMG) activity both contralateral (CSP: contralateral silent period) and ipsilateral (the " ipsilateral silent period" -IpSP). lpSP is a measure of interhemispheric motor inhibition that has been found to be altered in patient with MS and callosal lesions.

Compared to the separate recording of the EEG signals and those generated by the TMS, the simultaneous execution of the two methods - TMS-EEG - allows the recording directly from the scalp of the potentials (TEP) evoked by the TMS. The recording of TEPs from areas distant from the stimulation site allows to obtain information about the connectivity of the stimulated cortex. The "interhemispheric signal propagation" (ISP) is a measure of interhemispheric connectivity based on the propagation of TMS-EEG responses from the stimulated hemisphere to the contralateral. The ISP correlates with the microstructural integrity of the callosal microfibers and with the hand dexterity during motor development.

Neurophysiological estimates of grey matter Integrity:

Regarding gray matter (GM) pathology, evidences obtained from TMS and EEG studies have contributed to unveil the role of cortical dysfunction in MS. Alterations in EEG oscillations considered important in sensorimotor integration and motor control have been associated with clinical disorders and radiological changes in patients with MS. Furthermore, paired-pulse TMS protocols have shown alterations in M1 excitability in MS patients and that these alterations correlate with clinical disability. Among the measures of TMS-EEG, the locally recorded TEPs reflect the excitability and activation state of the stimulated cortex and therefore the degree of integrity of the cortical gray matter.

In conclusion, EEG and TMS-EEG measures are powerful tools to assess WM and GM functional integrity in patients with MS. As such, EEG and TMS-EEG also provide a potential objective framework to systematically assess the efficacy of Disease modifying therapies (DMTs) in MS.

Study aims and hypotheses Main aim of this study is the evaluation of TMS-EEG neurophysiological measures as surrogates of functional integrity of both gray and white matter in MS patients. The data obtained will be compared with those of a group of healthy subjects comparable for sex and age. Healthy subjects will be identified as those with normal neurological examination and negative medical history for morbidity. By combining the neurophysiological variables with the clinical ones, an attempt will be made to identify neurophysiological markers expressing the degree of disability of patients with MS (primary objective). The secondary objective is to identify the neurophysiological variables that may play a predictive role in the clinical or radiological relapses of the pathology and of the long-term clinical-radiological status. To this aim, the neurophysiological TMS-EEG measurements will be repeated longitudinally in the patients participating in the study and correlated with the clinical and radiological according to clinical practice. The neurophysiological markers identified may offer support in identifying patients in clinical deterioration or with a sub-optimal response to therapy.

Enrollment: To guarantee an adequate number of study participants and obtain data that are more traceable to real-life conditions, the investigators will collaborate in recruiting with other MS Centers (list with the relevant Managers attached). All neurophysiological evaluations will be performed at our Department and our Center will be the coordinator.

Tolerability of the neurophysiological evaluation The selected neurophysiological methods are non-invasive procedures, widely used and based on tools currently in use in clinical practice. These methods are painless and therefore easily implemented in a large population of subjects as they are safe and free of side effects.

Being tested
Neurophysiological assessment, clinical assessment
Keywords
neurophysiology, TMS-EEG, multiple sclerosis
Medical subject headings
Multiple Sclerosis, Demyelinating Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Neurophysiological assessmentOther

    EMG will be recorded from the Abductor pollicis brevis muscle (APB) with surface electrodes. EEG will be recorded with a 32-channel elastic cap via a TMS compatible system. TMS will be performed using a Magstim 200 stimulator with a 90 mm figure-of-eight coil localized on motor and non-motor areas using a neuronavigation system together with an optical tracking system. Coordinates for neuronavigation will be calculated in the MNI space and fit of each participant's anatomical MRI. Three minutes of continuous-EEG will be recorded with subjects at rest. Single-pulse neuronavigated TMS (sp-TMS) will be delivered at rest below the resting motor threshold intensity (RMT) over the APB hotspot on M1 during concurrent EEG recording. In a final block, the subject will maintain a voluntary muscle contraction (50% of the maximal voluntary contraction) of the left APB, and sp-TMS will be delivered at 130% RMT over the ipsilateral APB hotspot in order to record the lpSP.

  • clinical assessmentOther

    Clinical evaluation, performed at each time point, will include:

    • The assessment of clinical disability using EDSS score
    • The multiple sclerosis functional composite (MSFC), a three-part quantitative objective measure of neurologic function, measuring lower limbs (timed 25-foot walk [T25FW]), upper limbs (nine-hole peg test [9HPT]) and cognitive (three-second paced auditory serial addition test [PASAT3]) function.

    In order to reduce inter-rater variability, the same physician/technician with adequate training will administer all three tests. The patient should feel comfortable with the situation. Examiner should explain the instructions in a professional but friendly way and let the patient ask any questions before starting the tests. Examiner should write down the test results, as well as any situation that disturbs the performance of patient. Examiner should not provide direct feedback to the patient about his/her performance

Study groups in NCT04997343
Study groupRoleWhat they receive
MS patientsExperimentalAll MS patients will undergo clinical and neurophysiological evaluation at baseline (T0). The baseline will consider the radiological data of disease activity obtained from the most recently performed MRI according to clinical practice. These evaluations will be repeated according to clinical practice in patients taking DMT or every 6 months, in a stable condition or according to the indication of the treating neurologist in case of disease reactivation. A one-year neurophysiological, clinical and radiological observation is foreseen. Healthy subjects will undergo only the neurophysiological evaluation at baseline.
Receives: Other: Neurophysiological assessment; Other: clinical assessment
Healthy controlsOtherHealthy subjects will undergo only the neurophysiological evaluation at baseline.
Receives: Other: Neurophysiological assessment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes of Global cortico-cortical myelination

    Power of the dominant frequency peak of the global electroencephalography (EEG) signal.

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  2. Changes of the Cortical-cortical coherence

    Coherence between EEG signals recorded from distant channels.

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  3. Changes of the Local cortical-cortical myelination (motor)

    Power of the dominant frequency peak of the local EEG signal on primary motor cortex (M1).

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  4. Changes of the Trans-callosal axonal myelination

    Cortico-cortical coherence between EEG signals recorded on primary motor cortex (M1) areas bilaterally.

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  5. Changes of Interhemispheric signal propagation (iSP)

    TMS-EMG measurement of the ipsilateral silent period (IpSP)

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  6. Changes of TMS-EEG measurement of the functional integrity of the grey matter:

    Amplitude of the early components of Transcranial evoked potentials (TEPs).

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  7. Changes of TMS-EMG measurement of the functional integrity of the grey matter:

    Resting Motor Threshold- (RMT)

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  8. Changes of clinical outcome measures

    Clinical disability will be monitored with the Expanded Disability Status Scale (EDSS), performed by the same neurologist at each timepoint.

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  9. Changes of the Multiple Sclerosis Functional Composite (MSFC)

    To assess walking, lower limb functionality, upper limb dexterity and cognitive function.

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  10. Changes of radiological outcome measures

    Evaluation of the lesion load

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

  11. Changes of magnetic resonance imaging (MRI) number of lesions in T2

    Evaluation of new lesions in T2 compared to the previous evaluation.

    Measured: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Aug 2021
  2. Study startOct 2021 (estimated)
  3. Primary completion1 Jul 2023 (estimated)
  4. Study completion1 Sep 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
In this multicenter, longitudinal, interventional (for TMS-EEG) -observational (for clinical and radiological variables obtained according to clinical practice) case-control study, all participants will undergo clinical and neurophysiological evaluation at baseline (T0). The baseline will consider the radiological data of disease activity. These evaluations will be repeated according to clinical practice in patients taking Disease modifying therapies (DMTs) or every 6 months, in a stable condition or according to the indication of the treating neurologist in case of disease reactivation. A one-year neurophysiological, clinical and radiological observation is foreseen. Healthy subjects will undergo only the neurophysiological evaluation at baseline. For the study, no hospital diagnostic equipment will be used, but machinery present in the research laboratories, for research use only, bearing the CE mark.
Masking
None (open label)
Enrolment
128 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04997343
Sponsor's protocol ID
6357
Status last verified
Aug 2021
First submitted
12 Jul 2021
Last updated
9 Aug 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: all collected IPD will be shared at the end of the study by request from any qualified investigator.

Publications

  • Boniface SJ, Mills KR, Schubert M. Responses of single spinal motoneurons to magnetic brain stimulation in healthy subjects and patients with multiple sclerosis. Brain. 1991 Feb;114 ( Pt 1B):643-62. doi: 10.1093/brain/114.1.643.

    PubMed 2004261
  • Casula EP, Maiella M, Pellicciari MC, Porrazzini F, D'Acunto A, Rocchi L, Koch G. Novel TMS-EEG indexes to investigate interhemispheric dynamics in humans. Clin Neurophysiol. 2020 Jan;131(1):70-77. doi: 10.1016/j.clinph.2019.09.013. Epub 2019 Oct 24.

    PubMed 31756594
  • Conte A, Lenzi D, Frasca V, Gilio F, Giacomelli E, Gabriele M, Bettolo CM, Iacovelli E, Pantano P, Pozzilli C, Inghilleri M. Intracortical excitability in patients with relapsing-remitting and secondary progressive multiple sclerosis. J Neurol. 2009 Jun;256(6):933-8. doi: 10.1007/s00415-009-5047-0. Epub 2009 Mar 1.

    PubMed 19252788
  • Cutter GR, Baier ML, Rudick RA, Cookfair DL, Fischer JS, Petkau J, Syndulko K, Weinshenker BG, Antel JP, Confavreux C, Ellison GW, Lublin F, Miller AE, Rao SM, Reingold S, Thompson A, Willoughby E. Development of a multiple sclerosis functional composite as a clinical trial outcome measure. Brain. 1999 May;122 ( Pt 5):871-82. doi: 10.1093/brain/122.5.871.

    PubMed 10355672
  • Dobson R, Giovannoni G. Multiple sclerosis - a review. Eur J Neurol. 2019 Jan;26(1):27-40. doi: 10.1111/ene.13819. Epub 2018 Nov 18.

    PubMed 30300457
  • Ferrazzano G, Crisafulli SG, Baione V, Tartaglia M, Cortese A, Frontoni M, Altieri M, Pauri F, Millefiorini E, Conte A. Early diagnosis of secondary progressive multiple sclerosis: focus on fluid and neurophysiological biomarkers. J Neurol. 2021 Oct;268(10):3626-3645. doi: 10.1007/s00415-020-09964-4. Epub 2020 Jun 5.

    PubMed 32504180
  • Giovannoni G, Lang S, Wolff R, Duffy S, Hyde R, Kinter E, Wakeford C, Sormani MP, Kleijnen J. A Systematic Review and Mixed Treatment Comparison of Pharmaceutical Interventions for Multiple Sclerosis. Neurol Ther. 2020 Dec;9(2):359-374. doi: 10.1007/s40120-020-00212-5. Epub 2020 Sep 28.

    PubMed 32989721
  • Goodkin DE, Hertsgaard D, Seminary J. Upper extremity function in multiple sclerosis: improving assessment sensitivity with box-and-block and nine-hole peg tests. Arch Phys Med Rehabil. 1988 Oct;69(10):850-4.

    PubMed 3178453
  • Hallett M. Transcranial magnetic stimulation: a primer. Neuron. 2007 Jul 19;55(2):187-99. doi: 10.1016/j.neuron.2007.06.026.

    PubMed 17640522
  • Houdayer E, Comi G, Leocani L. The Neurophysiologist Perspective into MS Plasticity. Front Neurol. 2015 Sep 3;6:193. doi: 10.3389/fneur.2015.00193. eCollection 2015.

    PubMed 26388835
  • Jarczok TA, Fritsch M, Kroger A, Schneider AL, Althen H, Siniatchkin M, Freitag CM, Bender S. Maturation of interhemispheric signal propagation in autism spectrum disorder and typically developing controls: a TMS-EEG study. J Neural Transm (Vienna). 2016 Aug;123(8):925-35. doi: 10.1007/s00702-016-1550-5. Epub 2016 May 13.

    PubMed 27177879
  • Kurtzke JF. Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology. 1983 Nov;33(11):1444-52. doi: 10.1212/wnl.33.11.1444.

    PubMed 6685237
  • Lenzi D, Conte A, Mainero C, Frasca V, Fubelli F, Totaro P, Caramia F, Inghilleri M, Pozzilli C, Pantano P. Effect of corpus callosum damage on ipsilateral motor activation in patients with multiple sclerosis: a functional and anatomical study. Hum Brain Mapp. 2007 Jul;28(7):636-44. doi: 10.1002/hbm.20305.

    PubMed 17080438
  • Leocani L, Colombo B, Magnani G, Martinelli-Boneschi F, Cursi M, Rossi P, Martinelli V, Comi G. Fatigue in multiple sclerosis is associated with abnormal cortical activation to voluntary movement--EEG evidence. Neuroimage. 2001 Jun;13(6 Pt 1):1186-92. doi: 10.1006/nimg.2001.0759.

    PubMed 11352624
  • Leocani L, Rovaris M, Martinelli-Boneschi F, Annovazzi P, Filippi M, Colombo B, Martinelli V, Comi G. Movement preparation is affected by tissue damage in multiple sclerosis: evidence from EEG event-related desynchronization. Clin Neurophysiol. 2005 Jul;116(7):1515-9. doi: 10.1016/j.clinph.2005.02.026. Epub 2005 Apr 26.

    PubMed 15953556

Questions about this trial

What is this clinical trial studying?

A study testing Neurophysiological assessment and clinical assessment in people with Multiple Sclerosis and Demyelinating Disease, run by University of Roma La Sapienza.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 9 Aug 2021. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Antonella Conte, MD, PhD (00393466584811, antonella.conte@uniroma1.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes of Global cortico-cortical myelination (time frame: Baseline (T0) and at 6 and 12 months. Healthy controls will undergo only the neurophysiological evaluation at baseline.). The study lists 11 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04997343, which also lists 27 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Aug 2021.

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