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The National Amyotrophic Lateral Sclerosis Registry
Sponsor: Centers for Disease Control and Prevention
Summary
The purpose of this registry is to (A) better describe the incidence and prevalence of Amyotrophic Lateral Sclerosis (ALS) in the United States;(B) examine appropriate factors, such as environmental and occupational, that may be associated with the disease; (C) better outline key demographic factors (such as age, race or ethnicity, gender, and family history of individuals who are diagnosed with the disease) associated with the disease; and (D) better examine the connection between ALS and other motor neuron disorders that can be confused with ALS, misdiagnosed as ALS, and in some cases progress to ALS.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
30000
Start Date
2010-10
Completion Date
2040-12
Last Updated
2025-04-09
Healthy Volunteers
No
Conditions
Locations (1)
CDC
Atlanta, Georgia, United States