Studie

Low-Dos Fisetin Supplementation och Its Association With Chronic Inflammation i Middle-Aged och Older Adults: Studie Protocol for a Triple-Blind, Randomised, Placebo-Kontrollerad Trial.

Tavenier J, Berglind M, Hach LF, Christensen LWS, Masarikova MJ

RANDOMISERAD CONTROLLED TRIAL Nivå 2 2026

Triple-blind RCT protocol: 100 mg fisetin daily for 7 weeks i middle-aged och older adults, measuring plasma suPAR (inflammation). No results yet.

StudiedesignRANDOMISERAD CONTROLLED TRIAL
TierNivå 2, Strong humana bevis, hard endpoints or biomarkörer
År2026
TidskriftBasic & clinical pharmacology & toxicology
Publicerad2026 sep
Tillagd i NO1GEVITYaug 24, 2026

Tavenier et al. published a studie protocol for a triple-blind, randomiserad, placebokontrollerad trial of low-dos fisetin (100 mg orally once daily for 7 weeks) i middle-aged och older adults. The primär outcome is the between-group difference i change of plasma soluble urokinase plasminogen activator receptor (suPAR), a marker of chronic inflammation, från baseline till week 7. This is a protocol paper only — no results have been reported. Fisetin remains under clinical investigation as a senolytic och anti-inflammatory agent; the trial will add till the limited humana bevis base once completed.

Kritikernoter

Protocol only — no data, no effect size, no säkerhet results. Pending trial completion. Does not change fisetin evidensnivå (already C).

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