Under construction – not a live service
Sign in
Taking people in ItalyNo phase

Biomarkers of Synaptic Damage in Multiple Sclerosis

Key facts

Where
Pozzilli, ItalySee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Where in Italy

  • IRCCS NeuromedPozzilli, ItalyTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Neuromed IRCCS
Trial code
NCT03217396
Record updated
28 October 2022
Original description
A prospective and retrospective cohort study of about five years will be performed on blood and cerebrospinal fluid samples taken for diagnostic reasons from recruited patients within the Neuromed Neurology Unit. Subjects with other chronic neurodegenerative diseases such as Amyotrophic lateral sclerosis (ALS), Alzheimer's disease (AD) and Parkinson's disease (PD), and healthy subjects subjected to blood sampling and / or lumbar puncture for clinical reasons will be recruited As control groups.Read full original descriptionShow less

Identification of New Biomarkers Useful to Define the Course of Multiple Sclerosis and Study of the Mechanisms That Promote Synaptic Damage

A prospective and retrospective cohort study of about five years will be performed on blood and cerebrospinal fluid samples taken for diagnostic reasons from recruited patients within the Neuromed Neurology Unit. Subjects with other chronic neurodegenerative diseases such as Amyotrophic lateral sclerosis (ALS), Alzheimer's disease (AD) and Parkinson's disease (PD), and healthy subjects subjected to blood sampling and / or lumbar puncture for clinical reasons will be recruited As control groups.

Inclusion: Male and female patients (age between 18 and 65 years); Diagnosis of MS in accordance with McDonald's (2010 rev) criteria,; EDSS between 0 and 5.5 (included),; Patients able to provide informed consent to participation in the study.

Exclusion: Significant clinical conditions in addition to SM or other chronic neurodegenerative diseases including latent viral infections; Altered basal blood count; Inability to provide informed written consent; Pregnancy or lactation; Contraindications for the execution of magnetic resonance imaging with gadolinium.

ClinicalTrials.gov NCT03217396