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Sponsored by: |
National Institute on Aging (NIA) |
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Information provided by: | National Institute on Aging (NIA) |
ClinicalTrials.gov Identifier: | NCT00000178 |
This is a randomized placebo controlled, double blind study. Patients who meet eligibility criteria and decide to participate in the study will be randomly assigned to receive either drug treatment or a placebo. Neither the patients nor the participating investigators will know who is receiving the drugs and who is receiving the placebo. Participation involves 15 outpatient clinic visits over a 68 week period. Patients take study medication at varying doses (the maximum dose is 20 mg daily), along with calcium and vitamin supplements.
Condition | Intervention | Phase |
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Alzheimer Disease |
Drug: Prednisone |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Safety/Efficacy Study |
Official Title: | Multicenter Trial of Prednisone in Alzheimer's Disease |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Alabama | |
University of Alabama, Birmingham | |
Birmingham, Alabama, United States, 35294-0017 | |
United States, California | |
University of Southern California | |
Los Angeles, California, United States, 90033 | |
University of California, San Diego | |
San Diego, California, United States, 92093-0949 | |
United States, Florida | |
Mayo Clinic Jacksonville | |
Jacksonville, Florida, United States, 32225 | |
University of Miami | |
Miami, Florida, United States, 33140 | |
University of South Florida | |
Tampa, Florida, United States, 33162 | |
United States, Indiana | |
Indiana University Alzheimer's Center | |
Indianapolis, Indiana, United States, 46202 | |
United States, Kansas | |
University of Kansas Medical Center | |
Kansas City, Kansas, United States, 66160 | |
United States, Maryland | |
Johns Hopkins University | |
Baltimore, Maryland, United States, 21224 | |
United States, Minnesota | |
University of Minnesota | |
Minneapolis, Minnesota, United States, 55455 | |
United States, Missouri | |
Washington University | |
St. Louis, Missouri, United States, 63110 | |
United States, New York | |
Mount Sinai Medical Center | |
New York, New York, United States, 10029 | |
Columbia Presbyterian Medical Center | |
New York, New York, United States, 11032 | |
New York University Medical Center | |
New York, New York, United States, 10016 | |
University of Rochester | |
Rochester, New York, United States, 14620 | |
Burke Medical Research Institute | |
White Plains, New York, United States, 10605 | |
United States, Pennsylvania | |
University of Pittsburgh | |
Pittsburgh, Pennsylvania, United States, 15213 | |
United States, Tennessee | |
Vanderbilt University Medical Center | |
Nashville, Tennessee, United States, 37212-8646 | |
United States, Texas | |
University of Texas | |
Dallas, Texas, United States, 75235-9070 |
Principal Investigator: | Leon Thal, MD. | University of California, San Diego |
Study ID Numbers: | IA0002, 3U01AG10483-08S2 |
Study First Received: | October 29, 1999 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00000178 |
Health Authority: | United States: Federal Government |
Alzheimer's disease Prednisone Anti-inflammatory agents |
Prednisone Delirium, Dementia, Amnestic, Cognitive Disorders Mental Disorders Alzheimer Disease Central Nervous System Diseases |
Neurodegenerative Diseases Brain Diseases Dementia Cognition Disorders Delirium |
Anti-Inflammatory Agents Antineoplastic Agents, Hormonal Antineoplastic Agents Therapeutic Uses Physiological Effects of Drugs Nervous System Diseases |
Hormones, Hormone Substitutes, and Hormone Antagonists Tauopathies Hormones Glucocorticoids Pharmacologic Actions |