Tier 4 — mechanistic
Pilot Study of Fisetin to Improve Fatigue Among Older Adult Cancer Survivors
ClinicalTrials.gov trial registry record
2025
Bibliography
- Trial registry
- View on ClinicalTrials.gov Registered trial — results not yet published in a peer-reviewed journal.
- Funding
- Sponsor: Wake Forest University Health Sciences.
- Competing interests
- Not reported in the registry record.
Study snapshot
| Design | Prospective randomized double-blind placebo-controlled crossover pilot trial. |
|---|---|
| Model | Cancer survivors aged 65 years or older with self-reported fatigue. |
| Sample | Estimated enrollment: 60 participants. |
| Intervention | Participants receive fisetin or placebo on two consecutive days in each of two consecutive weeks, then cross over after a 14-day washout; the current public registry should be consulted for exact dispensing instructions. |
| Duration | Two 2-week treatment periods separated by a 14-day washout, with follow-up through 12 weeks. |
| Endpoints | Fatigue; Safety; Adherence; Exploratory blood biomarkers |
What the study showed, in plain terms
Key findings
What this study can and cannot tell us
Editorial review
Reviewed by the Biohack Blueprint research team
Last verified



