Grants and Contracts Details
Description
This is a Phase IIb multicenter, randomized, double-blind, placebocontrolled
study evaluating the efficacy and safety of prazosin in
approximately 186 Alzheimer’s disease (AD) participants with
disruptive agitation in long-term care (LTC)
The total active study duration is approximately 1.5 years,
including start-up, recruitment and follow-up periods.
The total duration of individual study participation is approximately
14 weeks.
Individual study participation consists of the following:
• Screening period up to 14 days.
• Duration of treatment of 12 weeks.
Status | Finished |
---|---|
Effective start/end date | 9/11/18 → 1/4/22 |
Funding
- University of California San Diego Health: $73,810.00
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