Massive ALS registry launches to uncover disease clues
NCT ID NCT01772602
First seen Apr 29, 2026 · Last updated May 05, 2026 · Updated 2 times
Summary
This study is creating a large national registry of people with ALS in the United States. Researchers will collect information from up to 30,000 participants to better understand how many people have the disease, who is affected, and what environmental or occupational factors might be linked to it. The goal is to gather knowledge, not to test a treatment.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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CDC
RECRUITINGAtlanta, Georgia, 30333, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Conditions
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