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Role of Neurofilment in Diagnosis of Multiple SclerosisNFLMSNCT06197841

Neurofilament Light Chain as Diagnostic and Prognostic Marker in naïve Multiple Sclerosis Patients

An observational study of Role of Neurofilment in Diagnosis of Multiple Sclerosis, run by Assiut University at 1 site in Egypt.

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 The sponsor has not verified this record for over two years, so it may be out of date.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

Neurofilament protein detected in the serum appears to be a good marker for the extent of active neurodegeneration. Chitinase may also be a good marker reflecting the degree of astrocyte activation, or damage in active lesions (Paul et al, 2018).These markers have some clinical value for diagnosis and monitoring of… Read more about this study

Who is it for?
Ages 16 to 60 yearsHealthy volunteers can take part
How many people
85 participants
Where
1 siteEgypt
Study dates
1 Dec 2023to Dec 2024
Phase
Observational
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 16 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Study population: Naïve Patients who will meet the inclusion and exclusion criteria of MS will be assessed in the 1st visit by direct interview followed by clinical examination and neuropsychological assessments as well as laboratory assessment. Baseline MRI scans will be obtained at the first visit and 12, months follow up. In the follow up visits every 6 months for 1and half year at least with assessment for all previous will be repeated to detect early signs of progression.

Who may be able to join

  • All patients newly diagnosed MS according to the 2017-McDonalds criteria.

Who cannot join

  • patients who are already diagnosed MS and under DMTs treatment
  • Presence of other disorder or on medications that may affect the neurological or cognitive disorders.
  • Patients failed to commit to the follow up visits and regular MRI scans
  • Patients refused to sign the written informed consent

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Ahmed El menshawy

    Asyut

Other trials in Egypt

About this study

Official title: Neurofilament Light Chain and Cognitive Impairment as Diagnostic and Prognostic Markers in naïve Multiple Sclerosis Patients

Neurofilament protein detected in the serum appears to be a good marker for the extent of active neurodegeneration. Chitinase may also be a good marker reflecting the degree of astrocyte activation, or damage in active lesions (Paul et al, 2018).These markers have some clinical value for diagnosis and monitoring of disease activity. NfL can be objectively measured and quantified, it is highly sensitive to neurodegenerative processes and its concentration changes as the disease worsens or improves (Disanto et al., 2017). Numerous studies have shown that NfL levels increase during MS relapses and correlate with MRI lesion development (Disanto et al., 2016, 2017; Novakova et al., 2017), disease activity, (Thebault et al., 2020). Cognitive impairment is common in the early stages of multiple sclerosis, mainly affecting attention, working memory, and information processing speed, but also memory, inhibition, and conceptualisation. Poor performance is common but remains subtle and does not significantly affect the quality of life at this stage. However, many studies shows that these deficits reflect the destruction both within and outside lesions, and that they may therefore be considered as a severity marker in the early stages of multiple sclerosis. (Lengenfelder et al., 2005).

The aim of the work is to detect the role of serum NFL and chitinase as biomarkers in the diagnosis and prognosis of newly diagnosed multiple sclerosis patients, and to estimate the incidence of cognitive impairment and their relationship with the NFL in newly diagnosed MS patients.

Read the detailed description

Many immunological studies have been performed with the aim to identify MS specific biomarkers and disease mechanisms and to find markers able to predict clinical disease course and outcome (Housley et al, 2015) Besides MRI and markers related to therapy (induction of blocking antibodies) or JC virus infection, they include markers for neurodegeneration, such as neurofilaments, markers for astrocytic activation (eg. chitinase or GFAP). Neurofilament protein detected in the serum or cerebrospinal fluid appears to be a good marker for the extent of active neurodegeneration, but this is not MS specific. Chitinase may be a good marker for active disease in RRMS, reflecting the degree of astrocyte activation, or damage in active lesions (Paul et al, 2018).These markers have some clinical value for diagnosis and monitoring of disease activity. Cognitive impairment is common in the early stages of multiple sclerosis, mainly affecting attention, working memory, and information processing speed, but also memory, inhibition, and conceptualisation. Poor performance is common but remains subtle and does not significantly affect the quality of life at this stage. However, many studies shows that these deficits reflect the destruction both within and outside lesions, and that they may therefore be considered as a severity marker in the early stages of multiple sclerosis. (Lengenfelder et al., 2005).Aim of the work The aim of the work is to detect the role of serum neurofilament light chain and chitinase as well as cognitive impairment as biomarkers in the diagnosis and prognosis of newly diagnosed multiple sclerosis patients, and to estimate the incidence of cognitive impairment and their relationship with the NFL in newly diagnosed MS patients.Study Design This study is a cross-sectional, prospective, observational study. Subjects All newly diagnosed cases With MS patients attending different MS unites in Assiut governorate will be recruited and all eligible patients will be included.

Inclusion criteria:

All patients newly diagnosed MS according to the 2017-McDonalds criteria.

Exclusion criteria:

  1. patients who are already diagnosed as MS and on treatment.
  2. Presence of other disorder or on medications that may affect the neurological or cognitive disorders.
  3. Patients failed to commit to the follow up visits and regular MRI scans
  4. Patients refused to sign the written informed consent

Patients who will meet the inclusion and exclusion criteria will be assessed in the 1st visit by direct interview followed by clinical examination and neuropsychological assessments as well as laboratory assessment. Baseline MRI scans will be obtained at the first visit and 12 months. In the follow up visits every 6 months for 1and half year at least with assessment for all previous will be repeated to detect early signs of progression.Study tools (in detail, e.g., lab methods, instruments, steps, chemicals, …):

Demographic data: age at presentation and age at onset, sex, education years and special habits Clinical data: duration of illness, until diagnosis number of relapses/year and their features.

Clinical assessment: EDSS, 9-hole pig test, 25-feet walking test.

Clinical rating scales :

Cognitive assessment using the Brief International Cognitive Assessment for Multiple sclerosis (BICAMS) with the Arabic validated version (8) that include:

Symbol Digit Modalities Test (SDMT) (Langdon et al. 2012) for evaluating the information processing speed.

California Verbal Learning Test (CVLT-II) for evaluating verbal learning and memory.

Brief Visual Memory Test (BVMT) for evaluating visual learning and memory.

Multiple sclerosis Quality of life MSQoL-54 questionnaire (10) with sub scales that measures physical function, role limitations-physical, role limitations-emotional, pain, emotional well-being, energy, health perceptions, social function, cognitive function, health distress, overall quality of life, and sexual function.

Hamilton depression rating-17-item version (HAM-D 17).

Laboratory investigation:

CSF Oligoclonal band, Serum light chain Neurofilament using PCR Research outcomes The primary outcome is the detection of neurofilament as diagnostic and prognostic inflammatory markers in newly diagnosed MS patients.

Secondary outcome measure is incidence of depression, cognitive impairment in newly diagnosed MS patients.

Follow up of each patient every 6 months using the same previous scales

Keywords
Naïve multiple sclerosis patients, cognitive impairment, Neurofilment light chain, Chitinase, diagnosis and predictor for outcome
Medical subject headings
Cognitive Dysfunction, Disease

What is being measured

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

  1. The primary outcome is the detection of neurofilament light chain as diagnostic and prognostic inflammatory markers in newly diagnosed MS patients.

    Assessment of the serum level of NFL at base line before starting DMT and correlate it with motor disability, cognitive impairment after one and half year

    Measured: 1 and half year

Secondary outcomes (1)
  1. Assessment of the incidence of cognitive impairment among naive multiple sclerosis patients and their correlation with neurofilment light chain

    Assessment of cognitive impairment of the MS Patients using BICAMS

    Measured: 1 and half year

Timeline

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

  1. First posted9 Jan 2024
  2. Study start1 Dec 2023
  3. Primary completion1 Dec 2024 (estimated)
  4. Study completionDec 2024 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
85 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06197841
Sponsor's protocol ID
Assiut University/Egypt
Acronym
NFLMS
Status last verified
Dec 2023
First submitted
26 Dec 2023
Last updated
9 Jan 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Khedr EM, Hassan MM, Ezzeldeen MY, El-Kady MS, El-Mokhtar MA, Shokry AE. Motor symptoms at onset and manual dexterity predict cognitive impairment in drug-naive individuals with multiple sclerosis. J Neuroimmunol. 2025 Apr 15;401:578571. doi: 10.1016/j.jneuroim.2025.578571. Epub 2025 Feb 25.

    PubMed 40022906

Questions about this trial

What is this clinical trial studying?

An observational study of Role of Neurofilment in Diagnosis of Multiple Sclerosis, run by Assiut University at 1 site in Egypt.

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 4 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 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The primary outcome is the detection of neurofilament light chain as diagnostic and prognostic inflammatory markers in newly diagnosed MS patients. (time frame: 1 and half year). 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 NCT06197841, which also lists 1 linked publication.

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 Jan 2024.

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