Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
Healthy Volunteers
NCT07195318

Fisetin Supplementation for Healthy Aging

Led by Ove Andersen · Updated on 2025-11-20

120

Participants Needed

1

Research Sites

521 weeks

Total Duration

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AI-Summary

What this Trial Is About

There is growing interest among the general population in preventive health interventions that can help mitigate age-related decline, reduce the risk of chronic diseases, and promote healthy aging. The use of nutritional supplements has been increasing and is especially high in older adults and healthier individuals. In response to this demand, a growing number of nutritional supplements are being advertised for their "anti-aging" properties, claiming to target molecular and cellular "hallmarks of aging", such as chronic inflammation, oxidative stress, and cellular senescence. However, the overwhelming majority of these claims stem from preclinical studies in animal models (e.g., C. elegans, mice), and there is extremely limited evidence for beneficial effects, effective doses, or safety profiles of these supplements in humans. Moreover, the lack of strict regulations in the nutritional supplement industry leads to wide differences in the quality and in the actual content of active substances between supplements, which could impact both their efficacy and safety. The investigators will conduct a clinical trial in healthy volunteers, who will receive supplementation with fisetin (100 mg) or placebo daily for 7 weeks. Participants will be examined at regular intervals during the study period. The investigators will then investigate whether fisetin supplementation is safe and evaluate its effect on measures of chronic inflammation, cellular senescence, aging, and general health.

CONDITIONS

Official Title

Fisetin Supplementation for Healthy Aging

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Middle-aged or older adult (≥50 years)
  • Able to cooperate cognitively
  • Able to read and understand Danish
Not Eligible

You will not qualify if you...

  • Unable or unwilling to take oral supplements
  • Use of anti-aging supplements within the past 30 days
  • Treatment with anti-aging medications (e.g., metformin, rapamycin, semaglutide) within the past 30 days
  • Use of anti-inflammatory medications within the past 30 days
  • Treatment with medications that may negatively interact with fisetin within the past 30 days
  • Vaccination within the past 14 days
  • Participation in another investigational drug or intervention study within the past year
  • Active cancer or current cancer treatment
  • Unstable or uncontrolled major disorders requiring regular hospital monitoring (cardiovascular, renal, endocrine, immunological, hepatic, or cancer)
  • Planned medical or surgical procedures during the study period
  • Known allergy or hypersensitivity to fisetin or placebo ingredients
  • Any condition deemed by the investigator to pose risk or prevent study completion

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

Department of Clinical Research, Copenhagen University Hospital Amager & Hvidovre

Hvidovre, Denmark, 2650

Actively Recruiting

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Research Team

J

Juliette Tavenier

CONTACT

L

Line Jee Hartmann Rasmussen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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