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Natural History and Clinical Features of Amyotrophic Lateral Sclerosis (ALS)

Natural History and Clinical Features of Amyotrophic Lateral Sclerosis (ALS)

Recruiting
100 years and younger
All
Phase N/A

With the development of supportive measures, the natural history of ALS has changed. Researchers compared the natural history of ALS patients from 1999-2004 and 1984-1998 and found that the median survival time was significantly longer in the former than in the latter (4.32 years vs. 3.22 years) and that the disease progression was slower in the former, even after adjusting for other confounding factors. Although previous studies have provided reference for the diagnosis and treatment of ALS, the etiology of ALS is still unknown, and the relevant clinical features and natural history of ALS still lack the verification of large samples. Therefore, the research on the natural history of ALS is of great significance to further increase the understanding of ALS and provide new evidence for the diagnosis and treatment of ALS.

Study details
    Myelopathy
    spinal cord disorders
    Amyotrophic Lateral Sclerosis
    spinal cord disorders

NCT04454892

Peking University Third Hospital

19 February 2024

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