NCT Number: NCT00000178
Multicenter Trial of Prednisone in Alzheimer's Disease
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.
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Notify MeKey information
Conditions
Age range
0 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
University of Alabama, Birmingham, Birmingham, Alabama, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients with Alzheimer's disease who are in stable medical condition
Exclusion criteria
- Patients with diabetes or severe osteoporosis
Treatment and study plan
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Lead sponsor
National Institute on Aging (NIA)
Nih
Registry information
Important dates
- First posted
- Nov 1, 1999
- Registry last updated
- Jun 24, 2005
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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