New ALS registry launches in thailand to map disease patterns
NCT ID NCT07175935
First seen Nov 01, 2025 · Last updated May 18, 2026 · Updated 27 times
Summary
This study is creating a national registry of 100 people with ALS in Thailand. Researchers will collect information on genetics, symptoms, and how the disease progresses over time. The goal is to better understand ALS in this population and build a foundation for future research. No new treatments are being tested.
Disclaimer
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the original study
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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: •••••@•••••
Locations
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King Chulalongkorn Memorial hospital, The Thai Red Cross Society
RECRUITINGPathum Wan, Bangkok, 10330, Thailand
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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