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Taking people in ItalyNo phase

Studying amyotrophic lateral sclerosis through biomarkers to understand its variability

Studies how biomarkers help group adults with amyotrophic lateral sclerosis by their symptoms.

Plain-language title generated from the registry record
Registry title: Biomarker-driven Phenotypic Dissection of Amyotrophic Lateral Sclerosis

Key facts

Where
Milan and Torino, ItalySee the 3 sites

Where in Italy

  • Ospedale San LucaMilan, ItalyTaking people
  • Ospedale San RaffaeleMilan, ItalyTaking people
  • AOU Città della Salute e della ScienzaTorino, 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
Istituto Auxologico Italiano
Trial code
NCT06318598
Record updated
7 May 2025
Original description
The goal of this observational study is to understand the clinical variability in a population of ALS patients using multidimensional biomarkers. The main questions it aims to answer are:Read full original descriptionShow less

Dissezione Fenotipica Guidata da Biomarcatori Della Sclerosi Laterale Amiotrofica/Biomarker-driven Phenotypic Dissection of Amyotrophic Lateral Sclerosis

The goal of this observational study is to understand the clinical variability in a population of ALS patients using multidimensional biomarkers. The main questions it aims to answer are:

* Which set of biomarkers explain genotypic-phenotypic correlations in ALS? * Which set of biomarkers can be used to subdivide the ALS population in homogeneous subgroups?

Participants will undergo:

* neurological evaluation * neurophysiological evaluation * neuropsychological evaluation * whole exome sequencing * biomarker measurement in CSF and plasma

Inclusion: diagnosis of ALS or other motor neuron disease; residence near the study centers.

Exclusion: refusal to participate to the study; unable/unwilling to perform follow-up visits.

ClinicalTrials.gov NCT06318598