Quercefit® (Quercetin Phytosome — Indena)

Sophora japonica
Evidence Level
Limited
6 Clinical Trials
7 Documented Benefits
2/5 Evidence Score

Quercefit® is Indena's (Italy) proprietary Quercetin Phytosome® — a 1:1 complex of quercetin with sunflower lecithin that solves quercetin's notorious bioavailability problem (<2% from food). In a 12-person crossover study run by the manufacturer, 500 mg of the phytosome complex (about 200 mg of quercetin) raised peak plasma quercetin about 20-fold and total exposure roughly 20-fold compared with 500 mg of unformulated quercetin. Sourced from Sophora japonica L. flower buds and HPLC-standardized to ~40% total quercetin. Human evidence is thin: one randomized double-blind trial in 66 Japanese adults with pollen allergy symptoms, one randomized double-blind trial in 78 adults reporting chronic fatigue, and open-label registry studies in asthma and in amateur triathletes run by the same Italian group. Non-GMO, gluten-free, and vegan.

Studied Dose 250 to 500 mg/day, about 100 to 200 mg quercetin, in the studies; the 1,000 mg/day senolytic figure comes from trials pairing quercetin with a prescription drug, not tested for this product.
Active Compound Quercetin Phytosome® (quercetin 1:1 with sunflower lecithin, HPLC-standardized to ~40% total quercetin; from Sophora japonica buds).

Benefits

Higher Blood Levels Than Unformulated Quercetin (Absorption, Not a Health Outcome)

The Phytosome® delivery system solves quercetin's poor water solubility — the main reason unformulated quercetin shows <2% absorption from food. In a single-dose randomized crossover study in 12 healthy volunteers, funded and authored by the manufacturer, 500 mg of Quercefit® (about 200 mg of quercetin) produced a peak plasma quercetin level about 20 times higher than 500 mg of unformulated quercetin (223 vs 11 ng/mL) and roughly 20 times the total exposure, and the 250 mg dose gave about half those values. A 2025 systematic review from Monash University pooling 31 human quercetin absorption studies also lists the lecithin phytosome at a 20.1-fold increase, though that figure is drawn from this same manufacturer study, so no independent laboratory has repeated the measurement. This translates to meaningful blood quercetin levels at supplemental doses that food simply cannot reach.

Nasal and Eye Allergy Symptoms in One Placebo-Controlled Trial

The only randomized, double-blind, placebo-controlled test is a 4-week Japanese trial in 66 adults with pollen-related symptoms: 200 mg of quercetin as the phytosome daily improved eye itching, sneezing, nasal discharge and sleep disturbance, and quality-of-life scores, against placebo. The asthma numbers usually quoted for this ingredient come from a separate 30-day open registry of 58 patients (30 supplemented, 28 on standard care only) with no placebo, no blinding and no randomization, so the size of that effect is not reliable. Asthma and allergic rhinitis are diagnosed conditions and nothing here replaces prescribed treatment.

Run Time and Recovery in One Unblinded Athlete Registry

Exercise performance and recovery in athletes: in non-professional triathletes, Quercefit® 250 mg twice daily reduced run time from start to finish by 11.3% (vs 3.9% in controls). Post-run muscle pain, cramps and recovery time were rated better and oxidative stress readings fell. This was a 2-week registry of 48 amateur triathletes who were not randomized (23 supplemented, 25 not), there was no placebo and no blinding, several outcomes were self-rated, and two authors work for the manufacturer, so treat it as a starting point rather than proof.

Lower Fatigue Scores in a Double-Blind Trial

In a 2-month double-blind, placebo-controlled trial, 78 adults with a mean age of 56 who reported chronic fatigue took 500 mg/day of quercetin phytosome or placebo. Fatigue Impact Scale scores fell 10.6 points further in the supplement group than in the placebo group, sleep quality and a short physical performance battery improved, and daily step counts rose by about 1,440. This is one trial, two of its authors work for the manufacturer, and no independent group has repeated it.

Antioxidant and Anti-Inflammatory Action

Antioxidant and anti-inflammatory action: quercetin is among the most potent dietary flavonoids for free-radical scavenging and inhibits the NF-κB pathway that drives chronic inflammatory cytokine production. With Quercefit® delivering far more quercetin to the bloodstream, the human measurements so far are limited to biomarkers: oxidative stress readings fell in two unblinded registry studies, and a 3-day study in 57 volunteers found a smaller skin wheal after a histamine injection. Falling oxidative stress readings are laboratory numbers, not a health outcome.

Mast Cell Stabilization and Histamine Modulation

Mast cell stabilization and histamine modulation: quercetin stabilizes mast cells, reducing the degranulation and histamine release that drive allergic responses. In an unblinded 3-day study of 57 healthy volunteers, the wheal and the redness after a histamine injection were smaller in the groups taking 250 mg/day and 500 mg/day than in untreated controls, with the larger dose giving the larger effect. It was published in Esperienze Dermatologiche in 2020 by the same Italian group that ran the asthma registry, it is not indexed in PubMed, the comparison group took nothing, and nobody was blinded.

Small Interaction Check With Blood Thinners and Metformin

One uncontrolled before-and-after study, published in Minerva Cardioangiologica in 2019, tested 62 patients in three groups: bleeding time in 30 people on aspirin, ticlopidine or clopidogrel after 10 days of Quercefit®, INR in 20 people on warfarin or dabigatran after 20 days, and blood glucose plus HbA1c in 12 people with diabetes on metformin after 20 days. None of those measurements changed significantly. There was no control group and no randomization, the groups are small and the exposure was short, so this lowers concern rather than settling it. Anyone taking these medicines should tell their doctor before starting.

Mechanism of action

1

Phytosome® Bioavailability Enhancement

Quercetin's near-zero oral absorption is driven by its extremely poor water solubility. Complexing quercetin 1:1 with sunflower-derived phosphatidylcholine forms a lipid-soluble Phytosome that crosses the intestinal mucosa much more efficiently. In 12 healthy volunteers, 500 mg of the phytosome complex (about 200 mg of quercetin) raised peak plasma quercetin about 20-fold (223 vs 11 ng/mL) and total exposure roughly 20-fold compared with 500 mg of unformulated quercetin, and the 250 mg dose gave about half those values. The study was run and authored by the manufacturer.

2

Mast Cell Stabilization

Quercetin inhibits IgE-triggered degranulation of mast cells, reducing the release of histamine, leukotrienes, and other mediators responsible for itching, sneezing, nasal discharge, and bronchoconstriction. The human evidence is one unblinded 3-day study in 57 volunteers in which the skin wheal after a histamine injection was smaller at 250 and 500 mg/day than in untreated controls.

3

NF-κB Pathway Inhibition

NF-κB is the master transcription factor driving production of pro-inflammatory cytokines including TNF-α, IL-6, and IL-1β. Quercetin inhibits NF-κB nuclear translocation and downstream cytokine production, This pathway work comes from cell and animal experiments. In people, the only inflammation-related readouts reported with this product are oxidative stress markers in unblinded registry studies.

4

Antioxidant / Free Radical Scavenging

Quercetin's catechol B-ring and 3-hydroxyl group make it one of the more chemically active flavonoid antioxidants, directly neutralizing reactive oxygen species and regenerating other antioxidants like vitamin C and glutathione. Oxidative stress markers improved in the unblinded triathlete registry, consistent with the in vitro free-radical scavenging activity scaling to the bloodstream when bioavailability is enhanced.

5

Histamine H1 Receptor Antagonism (Modest)

Quercetin shows modest binding affinity at H1 histamine receptors in vitro, adding to its anti-allergic profile beyond mast cell stabilization. The clinical effect is unlikely to approach pharmaceutical antihistamines, but contributes to the multi-mechanism profile that may explain symptomatic improvements observed in allergic rhinitis trials.

6

Antiviral Activity Seen Only in Laboratory Studies

Quercetin binds several viral targets in test-tube experiments, including the SARS-CoV-2 main protease. Laboratory binding is not a health claim. The COVID-19 studies of quercetin phytosome were open-label trials in patients already receiving medical care for a diagnosed infection, with no placebo and no blinding, and they are not a reason to take a supplement to prevent or treat any illness.

Clinical trials

1
Quercefit® Pharmacokinetic Trial — 20× Bioavailability vs Unformulated Quercetin
PubMed

Single-dose randomized three-way crossover pharmacokinetic study published in European Journal of Drug Metabolism and Pharmacokinetics. There was no placebo group: each volunteer acted as his or her own control, and all five authors are employees of Indena, which makes the ingredient. Compared Quercetin Phytosome® (Quercefit®, batch 06/16/PA) film-coated tablets given as 250 mg and 500 mg of the phytosome complex, which is about 40% quercetin by weight, against 500 mg of unformulated quercetin.

12 healthy adults aged 18 to 50, each receiving all three single doses in randomized order under fasting conditions.

Peak plasma quercetin was about 20 times higher with 500 mg of the phytosome complex than with 500 mg of unformulated quercetin (223 vs 11 ng/mL), and total exposure was about 20 times higher. The 250 mg dose produced about half those values, showing dose proportionality. Note that the 500 mg phytosome arm delivers only about 200 mg of quercetin, so the two arms are not matched on quercetin content. This study measures absorption only. It does not show that any health outcome improves, and it does not support dosing up to 1,000 mg/day, which no arm of it tested.

2
Open-Label Registry in Asthma With Rhinitis (No Placebo, Not Randomized)
PubMed

Open-label pilot registry published in Minerva Medica. Participants were not randomized and there was no placebo: subjects took the supplement alongside standard management or had standard management alone. 30-day intervention comparing Quercefit® 1-2 tablets/day (250-500 mg) plus standard management vs standard management alone, with outcomes assessed via the GINA classification system.

58 adults with mild-to-moderate asthma and allergic rhinitis: 30 took the supplement (20 of them at 200 mg/day quercetin, 10 at 100 mg/day) and 28 had standard management only.

Over 30 days the supplemented group had fewer daytime and nighttime symptoms, higher peak expiratory flow, less use of inhalers, nasal drops and rescue medication, a better rhinitis score and lower oxidative stress readings than the standard-care group. With no randomization, no placebo, no blinding and patient-reported symptom scores, the size of these differences cannot be taken at face value. The authors are the Chieti-Pescara group that has produced most of the published work on this ingredient.

3
Open-Label Registry in Amateur Triathletes (No Placebo, Not Randomized)
PubMed

Pilot registry study published in Minerva Medica, with no randomization, no placebo and no blinding. Two of the authors are Indena employees. Fourteen days of Quercefit® 250 mg twice daily (500 mg/day total) versus no supplement, across a training block of eight repeated sprint-distance runs.

48 amateur triathletes: 23 took the supplement and 25 did not.

Improvement in time to complete the run from baseline to day 14 was 11.3% in the supplemented group versus 3.9% in the controls. Post-run muscle pain, cramps and recovery time were rated better with the supplement and oxidative stress readings fell. Because the groups were self-selected rather than randomized and nobody was blinded, and because most of the recovery outcomes were rated by the athletes themselves, this is a preliminary signal from one 2-week study.

4
Open-Label COVID-19 Trial in Physician-Managed Outpatients (No Placebo)
PubMed

Randomized but open-label trial with no placebo, published in Frontiers in Pharmacology in 2023 and registered as NCT04861298, run at King Edward Medical University in Lahore. Patients received standard care plus 500 mg Quercetin Phytosome® three times daily in week one and twice daily in week two, or standard care alone. An interim analysis of the first 42 patients of this same trial was published separately in 2021, so those two papers describe one study, not two.

100 outpatients with mild-to-moderate COVID-19 receiving medical care (50 per group).

After one week, 34 of the 50 patients taking quercetin tested negative for SARS-CoV-2 versus 12 of 50 on standard care alone, 26 versus 12 had their acute symptoms resolve, and serum LDH fell from 407 to 258 U/L in the quercetin group. Nobody was blinded, the control group received no comparable tablet, and several of the authors are affiliated with the manufacturer. These were patients treated by doctors for a diagnosed infection. This is not a basis for using a supplement to prevent or treat COVID-19 or any other illness.

5
Quercefit® for Allergy Symptoms in Japanese Subjects
PubMed

Randomized, double-blind, placebo-controlled parallel-group trial published in European Review for Medical and Pharmacological Sciences in 2022. Four weeks of a supplement providing 200 mg of quercetin as Quercetin Phytosome®, or a matching vehicle, with symptoms scored on the Japanese Rhino-conjunctivitis Quality of Life Questionnaire. The authors are based at a Japanese university and a clinical research group, with no manufacturer employees on the paper.

66 Japanese adults with seasonal and/or perennial allergic symptoms.

Repeated oral Quercefit® reduced eye itching, sneezing, nasal discharge, and sleep disturbance for both seasonal and annual allergens vs placebo. Improved quality of life scores. This is the only double-blind, placebo-controlled allergy trial of this ingredient, it enrolled 66 people aged 22 to 78 with pollen-related symptoms, and no independent group has repeated it.

6
Uncontrolled Before-and-After Interaction Check (No Control Group)
PubMed

Uncontrolled before-and-after pilot study published in Minerva Cardioangiologica in 2019. Each participant was measured before and after supplementation, with no control group and no randomization. Evaluated potential interactions of Quercefit® with the antiplatelet agents acetylsalicylic acid, ticlopidine, and clopidogrel; anticoagulants warfarin and dabigatran; and glucose control in stable subjects.

62 patients in three separate groups: 30 on aspirin, ticlopidine or clopidogrel for 10 days, 20 on warfarin or dabigatran for 20 days, and 12 with diabetes on metformin for 20 days.

Quercefit® did not appear to alter the activity of any of the antiplatelet agents tested, had no impact on stable subjects using warfarin or dabigatran, and did not interfere with glycemic control. Bleeding time, INR, blood glucose and HbA1c all stayed at their baseline values. With 62 people in total, no control group and exposures of only 10 to 20 days, this lowers concern about these particular combinations without ruling an interaction out.

Side effects and drug interactions

Common Potential side effects

Generally very well tolerated across published trials at 250-1,000 mg/day.
Mild gastrointestinal upset (nausea, indigestion) reported uncommonly, typically with high doses on empty stomach.
Headache rare and usually transient.
Allergic reactions to quercetin itself are rare; the Quercefit® matrix uses sunflower lecithin (not soy) so soy allergy is not a concern.
Tingling/paresthesia at very high doses (>1,000 mg/day) has been anecdotally reported.
Kidney function: very high-dose long-term use (>1 g/day for extended periods) has theoretical kidney concern; clinical doses well below this threshold.

Important Drug interactions

Antiplatelet agents (aspirin, ticlopidine, clopidogrel) — the dedicated Quercefit® non-interference trial found no apparent interaction; routine medical supervision still advised.
Anticoagulants (warfarin, dabigatran) — the same Quercefit® safety trial reported no impact on stable patients; still monitor INR if combining with warfarin.
Diabetes medications — the Quercefit® non-interference trial reported no interference with glycemic control; monitor blood glucose if combining.
Cyclosporine — quercetin may increase cyclosporine plasma levels via CYP3A4 inhibition; clinically relevant interaction, requires medical supervision.
Quinolone antibiotics (ciprofloxacin, levofloxacin) — quercetin may compete for the same bacterial target and theoretically reduce antibiotic efficacy; separate doses by 2+ hours.
Chemotherapy agents — variable effects; some studies suggest quercetin may enhance certain agents while interfering with others. Discontinue and consult oncologist before use.
Pregnancy/lactation — quercetin from food (apples, onions, capers) considered safe; concentrated supplementation has limited safety data — avoid high-dose supplementation during pregnancy and lactation.

Frequently asked questions about Quercefit® (Quercetin Phytosome — Indena)

What is Quercefit?

Quercefit® is Indena's (Italy) proprietary Quercetin Phytosome® — a 1:1 complex of quercetin with sunflower lecithin that solves quercetin's notorious bioavailability problem (<2% from food).

What is Quercefit used for?

Quercefit is researched primarily for Respiratory Health, Antioxidant, and Athletic Performance. The Phytosome® delivery system solves quercetin's poor water solubility — the main reason unformulated quercetin shows <2% absorption from food.

What is the recommended dosage of Quercefit?

The clinically studied dose is 250 to 500 mg/day, about 100 to 200 mg quercetin, in the studies; the 1,000 mg/day senolytic figure comes from trials pairing quercetin with a prescription drug, not tested for this product. Always follow the product label and check with a healthcare provider for personal advice.

Is Quercefit safe, and does it have side effects?

For most healthy adults, Quercefit is well tolerated at studied doses. Reported effects can include: Generally very well tolerated across published trials at 250-1,000 mg/day. Mild gastrointestinal upset (nausea, indigestion) reported uncommonly, typically with high doses on empty stomach. It may also interact with some medications. Quercefit is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Quercefit interact with any medications?

Possible interactions include: Antiplatelet agents (aspirin, ticlopidine, clopidogrel) — the dedicated Quercefit® non-interference trial found no apparent interaction; routine medical supervision still advised. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Quercefit?

NutraSmarts rates the evidence for Quercefit as Limited (2 out of 5). It is backed by 6 clinical trials and 10 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(10 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Riva A, Ronchi M, Petrangolini G, Bosisio S, Allegrini P Improved Oral Absorption of Quercetin from Quercetin Phytosome, a New Delivery System Based on Food Grade Lecithin Eur J Drug Metab Pharmacokinet. 2019;44(2):169-177. doi: 10.1007/s13318-018-0517-3.PubMedUsed to support: Core pharmacokinetic evidence that Quercetin Phytosome (Quercefit) markedly raises quercetin bioavailability vs unformulated quercetin. Industry (Indena) PK study in healthy volunteers; the bioavailability advantage is the best-supported claim for this ingredient.
  2. Di Pierro F, Iqtadar S, Khan A, Ullah Mumtaz S, Masud Chaudhry M, Bertuccioli A, Derosa G, Maffioli P, Togni S, Riva A, Allegrini P, Khan S Potential Clinical Benefits of Quercetin in the Early Stage of COVID-19: Results of a Second, Pilot, Randomized, Controlled and Open-Label Clinical Trial Int J Gen Med. 2021;14:2807-2816. doi: 10.2147/IJGM.S318949.PubMedUsed to support: Interim report of the first 42 patients of the open-label randomized COVID-19 trial NCT04861298 at King Edward Medical University, Lahore. Patients receiving standard care plus Quercetin Phytosome (500 mg three times daily in week one, twice daily in week two) cleared SARS-CoV-2 sooner than those on standard care alone, and LDH, ferritin, CRP and D-dimer fell. There was no placebo and no blinding, Indena employees are among the authors, and the concluding 100-patient analysis of this same trial was published in Frontiers in Pharmacology in 2023.
  3. Di Pierro F, Derosa G, Maffioli P, Bertuccioli A, Togni S, Riva A, Allegrini P, Khan A, Khan S, Khan BA, Altaf N, Zahid M, Ujjan ID, Nigar R, Khushk MI, Phulpoto M, Lail A, Devrajani BR, Ahmed S Possible Therapeutic Effects of Adjuvant Quercetin Supplementation Against Early-Stage COVID-19 Infection: A Prospective, Randomized, Controlled, and Open-Label Study Int J Gen Med. 2021;14:2359-2366. doi: 10.2147/IJGM.S318720.PubMedUsed to support: Open-label randomized study in 152 COVID-19 outpatients in Pakistan given 1,000 mg/day of Quercetin Phytosome for 30 days alongside standard care. The authors report fewer and shorter hospitalisations, less need for oxygen and fewer deaths than in the control group, but there was no placebo and no blinding, Indena employees are among the authors and one declares a pending patent on quercetin phytosome, and the paper's own conclusion calls for a double-blind placebo-controlled study to confirm the findings.
  4. Cesarone MR, Belcaro G, Hu S, Dugall M, Hosoi M, Ledda A, Feragalli B, Maione C, Cotellese R Supplementary prevention and management of asthma with quercetin phytosome: a pilot registry Minerva Med. 2019;110(6):524-529. doi: 10.23736/S0026-4806.19.06319-5.PubMedUsed to support: Backs an anti-inflammatory/respiratory (asthma management) application of Quercetin Phytosome. Open-label pilot registry from the Belcaro group; preliminary supplement-study evidence.
  5. Riva A, Vitale JA, Belcaro G, Hu S, Feragalli B, Vinciguerra G, Cacchio M, Bonanni E, Giacomelli L, Eggenhöffner R, Togni S Quercetin phytosome® in triathlon athletes: a pilot registry study Minerva Med. 2018;109(4):285-289. doi: 10.23736/S0026-4806.18.05681-1.PubMedUsed to support: Open, non-randomized 14-day registry in 48 amateur triathletes (23 took 250 mg quercetin phytosome twice daily, 25 took nothing). Improvement in time to complete the training run was 11.3% with the supplement versus 3.9% in controls, and self-rated post-run pain, cramps, recovery time and oxidative stress readings were better. No placebo and no blinding, and two authors are employed by the manufacturer.
  6. Riva A, Corti A, Belcaro G, Cesarone MR, Dugall M, Vinciguerra G, Feragalli B, Zuccarini M, Eggenhoffner R, Giacomelli L Interaction study between antiplatelet agents, anticoagulants, diabetic therapy and a novel delivery form of quercetin Minerva Cardioangiol. 2019;67(1):79-83. doi: 10.23736/S0026-4725.18.04795-3.PubMedUsed to support: Uncontrolled before-and-after pilot study of Quercetin Phytosome in 62 patients: bleeding time was unchanged in 30 people taking aspirin, ticlopidine or clopidogrel after 10 days, INR was unchanged in 20 people on warfarin or dabigatran after 20 days, and glucose and HbA1c were unchanged in 12 people with diabetes on metformin after 20 days. There was no control group, the groups are small and the exposure was brief.
  7. Hickson LJ, Langhi Prata LGP, Bobart SA, Evans TK, Giorgadze N, Hashmi SK, et al. Senolytics decrease senescent cells in humans: Preliminary report from a clinical trial of Dasatinib plus Quercetin in individuals with diabetic kidney disease EBioMedicine. 2019;47:446-456. doi: 10.1016/j.ebiom.2019.08.069.PubMedUsed to support: Open-label phase 1 pilot in 9 people with diabetic kidney disease who took the prescription drug dasatinib 100 mg plus quercetin 1,000 mg for 3 days. Markers of senescent cells in fat and skin fell 11 days later. This is where the 1,000 mg senolytic quercetin dose comes from: it was given with a prescription drug, for 3 days, in a 9-person study, using plain quercetin rather than the phytosome, and it measured tissue markers rather than any health outcome.
  8. Yamada S, Shirai M, Inaba Y, Takara T Effects of repeated oral intake of a quercetin-containing supplement on allergic reaction: a randomized, placebo-controlled, double-blind parallel-group study Eur Rev Med Pharmacol Sci. 2022;26(12):4331-4345. doi: 10.26355/eurrev_202206_29072.PubMedUsed to support: Randomized, double-blind, placebo-controlled trial in 66 Japanese adults aged 22 to 78 with pollen-related allergic symptoms. Four weeks of a supplement providing 200 mg quercetin as Quercetin Phytosome improved Japanese Rhino-conjunctivitis Quality of Life Questionnaire scores for eye itching, sneezing, nasal discharge and sleep disturbance compared with placebo. This is the only blinded, placebo-controlled allergy trial of this formulation, and none of the authors is affiliated with the manufacturer.
  9. Di Pierro F, Khan A, Iqtadar S, Mumtaz SU, Chaudhry MNA, Bertuccioli A, Derosa G, Maffioli P, Togni S, Riva A, Allegrini P, Recchia M, Zerbinati N Quercetin as a possible complementary agent for early-stage COVID-19: Concluding results of a randomized clinical trial Front Pharmacol. 2023;13:1096853. doi: 10.3389/fphar.2022.1096853.PubMedUsed to support: Final report of the open-label randomized trial (NCT04861298) in 100 medically supervised COVID-19 outpatients in Lahore. Patients given standard care plus 500 mg Quercetin Phytosome three times daily for one week then twice daily for a second week were more often SARS-CoV-2 negative at one week (34 of 50 vs 12 of 50) and had lower serum LDH. There was no placebo and no blinding, and authors from the manufacturer are on the paper. The 2021 Int J Gen Med pilot reports the first 42 patients of this same trial.
  10. Rondanelli M, Riva A, Petrangolini G, Gasparri C, Perna S Two-month period of 500 mg lecithin-based delivery form of quercetin daily dietary supplementation counterbalances chronic fatigue symptoms: A double-blind placebo controlled clinical trial Biomed Pharmacother. 2023;167:115453. doi: 10.1016/j.biopha.2023.115453.PubMedUsed to support: Randomized, double-blind, placebo-controlled trial in 78 adults (mean age 56) reporting chronic fatigue. Two months of 500 mg/day quercetin phytosome lowered Fatigue Impact Scale scores by 10.58 points more than placebo, improved Pittsburgh Sleep Quality Index scores by 2.04 points, raised the short physical performance battery score by 0.25 points and increased daily steps by about 1,443. Two of the five authors are employed by the manufacturer, and the trial has not been independently repeated.