Viewing Study NCT01772602


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Study NCT ID: NCT01772602
Status: RECRUITING
Last Update Posted: 2025-04-09
First Post: 2013-01-17
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: The National Amyotrophic Lateral Sclerosis Registry
Sponsor: Centers for Disease Control and Prevention
Organization:

Study Overview

Official Title: The National Amyotrophic Lateral Sclerosis Registry
Status: RECRUITING
Status Verified Date: 2025-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.
Detailed Description: The National ALS Registry's Research Notification System allows person with ALS to participate in clinical trials.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: