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Genetic Epidemiology of Familial Amyotrophic Lateral Sclerosis (ALS)
This study is currently recruiting participants.
Verified by Emory University, December 2008
Sponsored by: Emory University
Information provided by: Emory University
ClinicalTrials.gov Identifier: NCT00317616
  Purpose

The investigators' long term goal is to undertake a clinical trial designed to investigate whether it is possible to delay or prevent the onset of disease amongst people at risk for developing familial ALS (fALS).

One of the major challenges we, the investigators at Emory University, face, as we consider the feasibility of a clinical trial, is how to predict who is at greatest risk for developing ALS within what time frame. In order to try to address this question, we invite all subjects to undergo genetic testing and to complete a short questionnaire regarding possible environmental risks (eg. smoking, pesticide exposure, military service and exercise) so that we can acquire more detailed information about individual and family histories. This information will then be correlated with the results of the genetic testing in order to develop statistical models to enable us to predict which subjects are at greatest risk for developing ALS. This information will help us decide if it is possible to plan a treatment trial in the future.

Results of genetic testing will not be given to participants.


Condition
Amyotrophic Lateral Sclerosis

Genetics Home Reference related topics: amyotrophic lateral sclerosis
MedlinePlus related topics: Amyotrophic Lateral Sclerosis
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective
Official Title: Genetic Epidemiology of Familial Amyotrophic Lateral Sclerosis

Further study details as provided by Emory University:

Biospecimen Retention:   Samples With DNA

Biospecimen Description:

Estimated Enrollment: 30
Study Start Date: April 2006
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Healthy individuals who harbor a mutation in the SOD1 gene.

Criteria

Inclusion Criteria:

  • Familial amyotrophic lateral sclerosis
  • Related to individuals with familial amyotrophic lateral sclerosis

Exclusion Criteria:

  • Under 18 years old
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00317616

Contacts
Contact: Sue Gronka, RN 888-413-9315 fALS@emory.edu

Locations
United States, Georgia
Emory University Recruiting
Atlanta, Georgia, United States, 30322
Sponsors and Collaborators
Emory University
Investigators
Principal Investigator: Michael Benatar, MD, PhD. Emory University
  More Information

Responsible Party: Emory University ( Michael Benatar )
Study ID Numbers: 1369-2005
Study First Received: April 24, 2006
Last Updated: December 23, 2008
ClinicalTrials.gov Identifier: NCT00317616  
Health Authority: United States: Institutional Review Board

Keywords provided by Emory University:
familial Amyotrophic Lateral Sclerosis
People with two or more family members diagnosed with ALS

Study placed in the following topic categories:
Amyotrophic lateral sclerosis
Neuromuscular Diseases
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Central Nervous System Diseases
Lou Gehrig's disease
Sclerosis
Degenerative motor system disease
Neurodegenerative Diseases
Motor neuron disease
Motor Neuron Disease

Additional relevant MeSH terms:
Pathologic Processes
Nervous System Diseases

ClinicalTrials.gov processed this record on January 16, 2009