Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease) Clinical Trials

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Biofluid Research on Age-Related or Inherited Neurodegeneration (BRAIN)

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The aim of this study is to contribute to and continue to sustain a repository of blood samples, nucleic acid (DNA and/or RNA) samples, family history information, and other demographic information from individuals with age-related neurodegenerative conditions, or their family members who may or may not be at risk for similar conditions. This study will continue to further expand research into the molecular and genetic basis of these diseases and their risk factors.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• People with a clinical diagnosis of a neurodegenerative disease including, but not limited to Alzheimer's disease (AD), Parkinson's disease (PD), Parkinson's disease dementia (PDD), dementia with Lewy bodies (DLB), frontotemporal dementia (FTD), amyotrophic lateral sclerosis (ALS), progressive supranuclear palsy (PSP), primary progressive aphasia (PPA), limbic-predominant age-related TDP-43 encephalopathy (LATE), corticobasal syndrome (CBS), posterior cortical atrophy (PCA), primary lateral sclerosis (PLS), primary muscular atrophy (PMA), or individuals with a suspected neurodegenerative dementia and/or movement disorder of unknown etiology will be considered for enrollment

• Family Members of individuals who meet the criteria of group 1, who are people who may or may not be at risk for a similar neurodegenerative disease, who may or may not be symptomatic, and who may or may not have known or unknown genetic risk.

• People with no known neurological disease who will provide control data.

Locations
United States
Pennsylvania
University of Pennsylvania
RECRUITING
Philadelphia
Contact Information
Primary
Cara Joyce, MPH
cara.joyce@pennmedicine.upenn.edu
267-271-0740
Backup
Emily Xie
emily.xie@pennmedicine.upenn.edu
16109553114
Time Frame
Start Date: 2025-12-12
Estimated Completion Date: 2070-01-01
Participants
Target number of participants: 1000
Treatments
People with a clinical diagnosis of neurodegenerative disease
People with a clinical diagnosis of a neurodegenerative disease including, but not limited to Alzheimer's disease (AD), Parkinson's disease (PD), Parkinson's disease dementia (PDD), dementia with Lewy bodies (DLB), frontotemporal dementia (FTD), amyotrophic lateral sclerosis (ALS), progressive supranuclear palsy (PSP), primary progressive aphasia (PPA), limbic-predominant age-related TDP-43 encephalopathy (LATE), corticobasal syndrome (CBS), posterior cortical atrophy (PCA), primary lateral sclerosis (PLS), primary muscular atrophy (PMA), or individuals with a suspected neurodegenerative dementia and/or movement disorder of unknown etiology will be considered for enrollment.
Family members of individuals meeting criteria for group 1
Family Members of individuals who meet the criteria of group 1, who are people who may or may not be at risk for a similar neurodegenerative disease, who may or may not be symptomatic, and who may or may not have known or unknown genetic risk.
Healthy Controls
People with no known neurological disease who will provide control data.
Sponsors
Collaborators: University of Pennsylvania Institute on Aging, National Institute on Aging (NIA), National Institute of Neurological Disorders and Stroke (NINDS)
Leads: University of Pennsylvania

This content was sourced from clinicaltrials.gov