Actively Recruiting
The National Amyotrophic Lateral Sclerosis Registry
Led by Centers for Disease Control and Prevention · Updated on 2026-04-29
30000
Participants Needed
1
Research Sites
1574 weeks
Total Duration
On this page
Sponsors
C
Centers for Disease Control and Prevention
Lead Sponsor
U
US Department of Veterans Affairs
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
The National Amyotrophic Lateral Sclerosis Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- U.S. citizens 18 years of age or older
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CDC
Atlanta, Georgia, United States, 30333
Actively Recruiting
Research Team
P
Paul Mehta, MD
CONTACT
K
Kevin Horton, DrPH, MSPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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