Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
240

Summary

Conditions
Alzheimer's Disease
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 50 years and 125 years
Gender
Both males and females

Description

This study uses a simple validated measure of brain atrophy as a surrogate marker in a repurposing effort that could recast an antihypertensive medication as a cognitive enhancer/neuroprotective agent and possibly as a drug of choice for Alzheimer patients and patients at risk for AD. If the proof o...

This study uses a simple validated measure of brain atrophy as a surrogate marker in a repurposing effort that could recast an antihypertensive medication as a cognitive enhancer/neuroprotective agent and possibly as a drug of choice for Alzheimer patients and patients at risk for AD. If the proof of concept result is positive, a larger study would be warranted with potential practice-changing impact.

Tracking Information

NCT #
NCT02085265
Collaborators
  • Alzheimer's Drug Discovery Foundation
  • Weston Brain Institute
Investigators
Principal Investigator: Sandra Black, MD Sunnybrook Health Sciences Centre Principal Investigator: Krista Lanctot, PhD Sunnybrook Research Institute