Actively Recruiting

Phase 2
Age: 60Years +
All Genders
NCT07279714

Fisetin in Mild Alzheimer's Disease

Led by Sunnybrook Health Sciences Centre · Updated on 2026-04-13

5

Participants Needed

1

Research Sites

39 weeks

Total Duration

On this page

Sponsors

S

Sunnybrook Health Sciences Centre

Lead Sponsor

S

Sunnybrook Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

This pilot study will evaluate the safety and tolerability of the natural health product, fisetin, in older adults with mild cognitive impairment or mild Alzheimer's disease dementia.

CONDITIONS

Official Title

Fisetin in Mild Alzheimer's Disease

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Mild cognitive impairment due to Alzheimer's disease or mild Alzheimer Dementia
  • Moca score of 11 or higher
  • Stable psychotropics and cognitive enhancing medications
Not Eligible

You will not qualify if you...

  • Known hypersensitivity or allergy to fisetin
  • Any medical condition or abnormal routine blood test that would put the subject at risk or prevent completing the trial
  • Unstable medical disorders
  • Ongoing treatment for active infection with antibiotics or antifungals
  • Ongoing treatment for cancer
  • Active alcohol or substance use disorder
  • Recent active bleeding
  • Taking oral anticoagulants, anti-cancer, anti-seizure medications, or other drugs that may interact significantly with fisetin
  • Use of other senolytic supplements, antioxidant supplements, or natural health products within the last month
  • Other neurologic or neurodegenerative conditions affecting cognition
  • Active Major Depressive Episode, active suicidal thoughts, or psychosis
  • Any condition preventing the ability to undergo an MRI scan

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sunnybrook Research Institute

Toronto, Ontario, Canada, M4N 3M5

Actively Recruiting

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Research Team

S

Study Coordinator

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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