Tier 4 — mechanistic
COVID-FISETIN: Pilot in SARS-CoV-2 of Fisetin to Alleviate Dysfunction and Inflammation in Hospitalized Adults
ClinicalTrials.gov trial registry record
2020
Bibliography
- Trial registry
- View on ClinicalTrials.gov Registered trial — results not yet published in a peer-reviewed journal.
- Funding
- Sponsor: Mayo Clinic.
- Competing interests
- Registry record; no results manuscript is available for a manuscript-level conflict-of-interest statement.
Study snapshot
| Design | Phase 2 randomized double-blind placebo-controlled parallel trial. |
|---|---|
| Model | Hospitalized adults aged 18 years and older with SARS-CoV-2 infection. |
| Sample | Target enrollment: 80 participants. |
| Intervention | Fisetin approximately 20 mg/kg/day orally or by enteral tube for two consecutive days versus placebo. |
| Duration | Two-day treatment course with inpatient clinical follow-up; registry listed primary/study completion around September 2026. |
| Endpoints | Oxygenation status; Progression to supplemental oxygen or assisted ventilation; COVID-19 disease severity; Inflammatory outcomes; Physical function/frailty; Safety and tolerability |
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



