New study aims to unlock ALS mysteries by tracking brain chemicals over time
NCT ID NCT07312240
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 140 adults with ALS for up to 3 years, collecting spinal fluid and blood samples along with clinical and cognitive tests. The goal is to understand how certain biological markers relate to different forms of the disease and its progression. This is an observational study, not a treatment trial, so participants will not receive any experimental therapy.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 140 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria ALS patients: * diagnosis of Amyotrophic Lateral Sclerosis (ALS); * age ≥18 y; * feasibility of lumbar puncture (LP); * informed consent. Exclusion Criteria ALS patients: * severe medical comorbidities; * recent traumatic, inflammatory, vascular, or neoplastic Central Nervous System disease; contraindications to LP. Inclusion Criteria Controls: * age ≥18 y; * individuals undergoing LP for neurological symptoms; * no evidence of nervous system pathology; * informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Istituto Auxologico Italiano IRCCS
RECRUITINGMilan, Lombardy, 20149, Italy
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