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Search / Trial NCT00040378

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

Alzheimer Disease Vitamin E Selenium

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.

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

0 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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