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Risk Factors for Progressive Supranuclear Palsy (PSP)

This study is currently recruiting participants.
Verified by University of Louisville, November 2007

Sponsors and Collaborators: University of Louisville
National Institute on Aging (NIA)
Information provided by: University of Louisville
ClinicalTrials.gov Identifier: NCT00431301
  Purpose

Progressive supranuclear palsy (PSP) is the most common atypical parkinsonian movement disorder. This study will determine the role of specific genetic, occupational and environmental components in the development of PSP by evaluating patients with this disorder and age and gender matched controls.


Condition
Progressive Supranuclear Palsy

MedlinePlus related topics:   Movement Disorders   Paralysis   Progressive Supranuclear Palsy  

U.S. FDA Resources

Study Type:   Observational
Study Design:   Case Control, Prospective
Official Title:   Genetic and Environmental Risk Factors for PSP

Further study details as provided by University of Louisville:

Biospecimen Retention:   Samples With DNA

Biospecimen Description:

DNA will be used for genotyping specific genes of interest related to the disease.


Estimated Enrollment:   1500
Study Start Date:   August 2006
Estimated Study Completion Date:   August 2010

Detailed Description:

This proposal will determine: (1) if there is an association between PSP and specific genes of interest; (2) if there is an association between PSP and occupational and/or environmental chemical exposures functionally or structurally similar to known parkinsonian toxicants; and (3) if hypertension or traumatic brain injury prior to symptom-onset is associated with PSP. To disentangle the complex etiology of PSP, this case-control multicenter study involves 500 PSP cases, 500 age/gender matched primary controls, and 500 secondary controls for genetic confirmation. Understanding the etiology of PSP may also help explain the causes of other related diseases such as Alzheimer's disease. This multidisciplinary team of movement disorder specialists, epidemiologists, geneticists, biostatisticians, industrial hygienist and toxicologist is well suited to unravel the etiology of PSP.

  Eligibility
Ages Eligible for Study:   40 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample

Study Population

Patients with clinically diagnosed Progressive Supranuclear Palsy and healthy controls


Criteria

Inclusion Criteria:

  • PSP patients able to visit one of the screening sites for diagnostic confirmation and able to participate in a one hour telephone interview

Exclusion Criteria:

  • No other major neurological disorders
  • Unable to communicate by telephone
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00431301

Contacts
Contact: Christopher Cunningham, Ph.D.     1-866-PSP-0448    
Contact: Casey Shepherd, M.P.H.     1-866-PSP-0448    

Locations
United States, Alabama
University of Alabama, Birmingham     Recruiting
      Birmingham, Alabama, United States, 35233
      Contact: Jennifer Newsome     205-996-7499        
      Principal Investigator: David Standaert, M.D., Ph.D.            
United States, California
UCLA     Recruiting
      Los Angeles, California, United States, 90095-1759
      Contact: Angeline Lo     310-206-2669        
      Principal Investigator: Yvette Bordelon, M.D.            
United States, Florida
Mayo Clinic Jacksonville     Withdrawn
      Jacksonville, Florida, United States, 32224
United States, Georgia
Emory College of Medicine     Recruiting
      Atlanta, Georgia, United States, 30322
      Contact: Carol Ingram     404-728-6859        
      Principal Investigator: Jorge Juncos, M.D.            
United States, Kentucky
University of Louisville     Recruiting
      Louisville, Kentucky, United States, 40202
      Contact: Chris Cunningham, Ph.D.     866-777-0448        
      Contact: Casey Shepherd, M.P.H.     502-852-3655        
      Principal Investigator: Irene Litvan, M.D.            
United States, Maryland
University of Maryland     Recruiting
      Baltimore, Maryland, United States, 21201
      Contact: Maura Deeley     410-328-7816        
      Principal Investigator: Stephen Reich, M.D.            
United States, Ohio
Case Western University     Recruiting
      Cleveland, Ohio, United States, 44106
      Contact: David Korosec     216-844-1800        
      Principal Investigator: David Riley, M.D.            
United States, Texas
Baylor College of Medicine     Active, not recruiting
      Houston, Texas, United States, 77030

Sponsors and Collaborators
University of Louisville
National Institute on Aging (NIA)

Investigators
Principal Investigator:     Irene Litvan, M.D.     University of Louisville    
  More Information

PSP study information website  This link exits the ClinicalTrials.gov site
 

Study ID Numbers:   1 R01 AG024040-01A2, 1 R01 AG024040-01A2
First Received:   February 1, 2007
Last Updated:   November 8, 2007
ClinicalTrials.gov Identifier:   NCT00431301
Health Authority:   United States: Institutional Review Board

Keywords provided by University of Louisville:
Progressive Supranuclear Palsy  
Epidemiology  
Case-Control  
Genetic  
Environmental  
Neurodegenerative Disease  
Movement Disorders
Atypical Parkinsonism
Parkinson Plus
Steele-Richardson-Olszewski
PSP

Study placed in the following topic categories:
Motor neuro-ophthalmic disorders
Ganglion Cysts
Basal Ganglia Diseases
Central Nervous System Diseases
Neurodegenerative Diseases
Brain Diseases
Ocular motility disorders
Paralysis
Ocular Motility Disorders
Parkinson Disease
Movement Disorders
Supranuclear Palsy, Progressive
Progressive supranuclear palsy
Neurologic Manifestations
Parkinsonian Disorders

Additional relevant MeSH terms:
Signs and Symptoms
Eye Diseases
Nervous System Diseases
Cranial Nerve Diseases
Tauopathies
Ophthalmoplegia

ClinicalTrials.gov processed this record on July 03, 2008




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