drugset / Trial / NCT00000178
Multicenter Trial of Prednisone in Alzheimer's Disease
RandomizedDouble-blindTreatment
Summary
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.
Timeline
- Start
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- Primary completion
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- Completion
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Outcome
Missed primary endpoint
paper There was no difference in cognitive decline between the prednisone and placebo treatment groups in the primary intent-to-treat analysis PMID 10680787 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Prednisone | Other / unclassified | 10 mg | — |