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RECRUITING
NCT01772602

The National Amyotrophic Lateral Sclerosis Registry

Sponsor: Centers for Disease Control and Prevention

View on ClinicalTrials.gov

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

Locations (1)

CDC

Atlanta, Georgia, United States