Skip to content
Pharma Observatory a Scientist.com platform

Clinical trial

Identification of Genes Causing Familial ALS or Increasing Risk for Sporadic ALS and ALS With Frontotemporal Dementia and Understanding Disease Mechanism.

NCT00821132 is registered in ClinicalTrials.gov with Northwestern University as lead sponsor.

NCT NCT00821132
Email me this page as a PDF

Search trials, sites, companies and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.

Get the NCT00821132 report as a PDF

The PDF carries up to 50 rows of each section, where the page shows the first few, with the sources listed. Enter a work email and confirm it from the message we send, and the report follows by email.

Registry record

As filed in ClinicalTrials.gov.

Title
Identification of Genes Causing Familial ALS or Increasing Risk for Sporadic ALS and ALS With Frontotemporal Dementia and Understanding Disease Mechanism.
Lead sponsor
Northwestern University
Phase
Observational
Overall status
Completed
Start date
January 31, 1991
Completion date
January 31, 2023
Enrollment
13,521 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

als with frontotemporal dementia (als/ftd), amyotrophic lateral sclerosis (als), familial amyotrophic lateral sclerosis, lou gehrig's disease, motor neuron disease (mnd), primary lateral sclerosis (pls), sporadic als (sals)