Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Mild Cognitive Impairment
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Open-label study with atorvastatin 40 mgMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 60 years and 95 years
Gender
Both males and females

Description

Participants are first being informed about potential benefits and risks of the study and are required to give written consent. After that participants will undergo detailed phone screen to determine eligibility for study entry. At week 0, participants who meet eligibility requirements will be presc...

Participants are first being informed about potential benefits and risks of the study and are required to give written consent. After that participants will undergo detailed phone screen to determine eligibility for study entry. At week 0, participants who meet eligibility requirements will be prescribed atorvastatin (40 mg, once in the evening) in an open-label manner.

Tracking Information

NCT #
NCT04765137
Collaborators
Not Provided
Investigators
Principal Investigator: Sevil Yasar, MD, PhD Johns Hopkins University