Prevention of Alzheimer's Disease by Vitamin E and Selenium (PREADVISE)
Launched by FREDERICK SCHMITT · Jun 26, 2002
Trial Information
Current as of May 29, 2025
Completed
Keywords
ClinConnect Summary
Studies show that increased oxidative stress (from excess free radicals) may damage brain cells and is linked with Alzheimer's disease (AD). Many studies show increased oxidation of brain lipids (fats), proteins, carbohydrates (sugars) and DNA in AD. Although the causes of AD are not known, it is believed that oxidative stress is part of what damages brain cells in AD and probably other brain diseases. Animal and tissue culture studies of vitamin E and selenium suggest that they can protect brain cells from damage. This research study is being done to see how safe and effective vitamin E an...
Gender
MALE
Eligibility criteria
- Inclusion Criteria:
- • Participating in SELECT Prevention study;
- • 62 years or older if other ethnic origin, or 60 years or older if African-American or Hispanic;
- • General good health with no neurological or psychiatric illness.
- Exclusion Criteria:
- The SELECT doctors or staff will review the PREADVISE applicants' medical history and drugs to verify that they have no condition(s) that would exclude them from this study. The participant must not have any of the following neurological conditions based on self report (were told by a physician):
- • Alzheimer's disease, or any other form of dementia such as Pick's disease, dementia with Lewy bodies, frontotemporal dementia, vascular dementia, significant cognitive and motor impairment from a stroke or corticobasal degeneration;
- • Huntington's disease, epilepsy, Parkinson's disease, brain tumor, multiple sclerosis, manic-depressive disorder, or schizophrenia;
- • The participant must not have had a head injury with prolonged loss of consciousness (over 30 minutes) within the past five years;
- • The participant must not have a current alcohol or substance abuse diagnosis, or must have been treatment free for the past 24 months;
- • The participant must not have had a diagnosis of depression or anxiety disorder in the past 4 months and must not currently be under treatment for depression or anxiety disorder. \[A participant who was previously diagnosed with depression or anxiety disorder but completed treatment more than four months ago is eligible.\];
- • The participant must not currently use of any of the following medications: Aricept, Cognex, Exelon, Reminyl, or Hydergine;
- • The participant must not have blindness, deafness, language difficulties or any other disability that may prevent completion of the memory screen.
About Frederick Schmitt
Frederick Schmitt is a distinguished clinical trial sponsor known for his commitment to advancing medical research and improving patient outcomes. With a robust background in neuroscience and clinical trial management, he leads initiatives focused on innovative therapeutic approaches, particularly in neurodegenerative diseases. His dedication to rigorous scientific standards and ethical practices ensures the integrity of research processes, fostering collaboration among academic institutions, healthcare professionals, and industry partners. Through his leadership, Frederick Schmitt strives to bridge the gap between cutting-edge research and practical application, ultimately enhancing the quality of care in the medical community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Kansas City, Kansas, United States
Washington, District Of Columbia, United States
Detroit, Michigan, United States
Springfield, Missouri, United States
Allentown, Pennsylvania, United States
Abington, Pennsylvania, United States
Anchorage, Alaska, United States
Red Bank, New Jersey, United States
Knoxville, Tennessee, United States
Toledo, Ohio, United States
Phillipsburg, New Jersey, United States
Sioux City, Iowa, United States
Fremont, Ohio, United States
Oregon, Ohio, United States
Anchorage, Alaska, United States
Ottawa, Ontario, Canada
Davenport, Iowa, United States
Northridge, California, United States
Joplin, Missouri, United States
Doylestown, Pennsylvania, United States
Washington, District Of Columbia, United States
Springfield, Missouri, United States
Nashville, Tennessee, United States
Omaha, Nebraska, United States
Seattle, Washington, United States
Glens Falls, New York, United States
Columbus, Ohio, United States
La Jolla, California, United States
Wichita, Kansas, United States
Billings, Montana, United States
Seattle, Washington, United States
Birmingham, Alabama, United States
Chula Vista, California, United States
Glendale, California, United States
La Jolla, California, United States
Loma Linda, California, United States
Long Beach, California, United States
Santa Rosa, California, United States
Torrance, California, United States
Upland, California, United States
Fort Collins, Colorado, United States
Washington, District Of Columbia, United States
Jacksonville, Florida, United States
Tucker, Georgia, United States
Ames, Iowa, United States
Cedar Rapids, Iowa, United States
Des Moines, Iowa, United States
Topeka, Kansas, United States
Wichita, Kansas, United States
Ashland, Kentucky, United States
Lexington, Kentucky, United States
Louisville, Kentucky, United States
Annapolis, Maryland, United States
Pittsfield, Massachusetts, United States
Adrian, Michigan, United States
Grand Rapids, Michigan, United States
Monroe, Michigan, United States
Pontiac, Michigan, United States
Traverse City, Michigan, United States
Duluth, Minnesota, United States
Great Falls, Montana, United States
Kearney, Nebraska, United States
Lincoln, Nebraska, United States
Omaha, Nebraska, United States
Omaha, Nebraska, United States
Reno, Nevada, United States
East Orange, New Jersey, United States
Albany, New York, United States
Cooperstown, New York, United States
Cincinnati, Ohio, United States
Maumee, Ohio, United States
Sylvania, Ohio, United States
Toledo, Ohio, United States
Toledo, Ohio, United States
Toledo, Ohio, United States
Muskogee, Oklahoma, United States
Bethlehem, Pennsylvania, United States
York, Pennsylvania, United States
Sioux Falls, South Dakota, United States
Memphis, Tennessee, United States
Oak Ridge, Tennessee, United States
Dallas, Texas, United States
Temple, Texas, United States
Bellingham, Washington, United States
Seattle, Washington, United States
Marshfield, Wisconsin, United States
Milwaukee, Wisconsin, United States
San Juan, , Puerto Rico
San Juan, , Puerto Rico
San Juan, , Puerto Rico
San Juan, , Puerto Rico
San Juan, , Puerto Rico
San Juan, , Puerto Rico
Patients applied
Trial Officials
Frederick Schmitt, PhD
Principal Investigator
Sanders-Brown Center on Aging
Richard Kryscio, PhD
Principal Investigator
Sanders-Brown Center on Aging
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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