Scientists hunt for genetic clues in ALS and related disorders
NCT ID NCT04875416
First seen Apr 05, 2026 · Last updated May 16, 2026 · Updated 5 times
Summary
This study aims to learn more about ALS and similar diseases like frontotemporal dementia and hereditary spastic paraplegia. Researchers will look at how a person's genetic makeup relates to their symptoms and will search for biological markers (biomarkers) in blood and spinal fluid. About 217 participants with these conditions will be observed over time, but no new treatments or drugs are being tested.
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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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Locations
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University of Cape Town
Cape Town, South Africa
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University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
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University of Miami
Miami, Florida, 33136, United States
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
Conditions
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