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Flavonoid

Quercetin for Coronary Artery Disease (Q-CABG Trial)

Phase 2
Waitlist Available
Led By Michel Carrier, MD
Research Sponsored by Montreal Heart Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
To have had a myocardial infarction (MI) within the past 30 days or to be in a state of stable angina before the surgery
Be hospitalized and waiting for a cardiac surgery of revascularization
Must not have
To have a past history of breast cancer or other tumors estrogen-dependent
Need for a quinolone during post-op
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 to 12 weeks post-surgery

Summary

This trial is testing quercetin, a natural substance found in fruits and vegetables, to see if it can reduce inflammation and slow down aging cells in patients undergoing heart bypass surgery. Patients will take quercetin starting before their surgery and continue for a short period afterward. The study will measure inflammation and cell health through blood samples. Quercetin is known for its antioxidant, anti-inflammatory, and cardio-protective properties.

Who is the study for?
This trial is for adults who've had a heart attack in the last 30 days or have stable angina, awaiting coronary artery bypass surgery. They must speak French or English and consent to participate. Excluded are those without recent heart attacks, with infections, severe kidney/liver disease, estrogen-dependent tumor history, flavonoid intolerance, or taking certain medications.
What is being tested?
The study examines Quercetin's potential to reduce inflammation and slow cell aging during coronary bypass surgery compared to a placebo. Participants will be randomly assigned to receive either Quercetin or an inactive substance.
What are the potential side effects?
Quercetin may cause side effects such as headaches and tingling of the extremities; digestive discomfort like acid reflux and diarrhea; and could potentially interact with various medications.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I had a heart attack in the last 30 days or my chest pain is stable.
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I am hospitalized and waiting for heart bypass surgery.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have had breast cancer or another estrogen-dependent tumor before.
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I need to take a quinolone antibiotic after surgery.
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My liver tests are more than twice the normal values.
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I cannot speak French or English.
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I am having another heart surgery along with my bypass surgery.
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I have been diagnosed with cirrhosis.
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My kidney function is low (GFR below 30).

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 1 day and 4 days post-surgery
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 1 day and 4 days post-surgery for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Quercetin-associated change in surgery-associated inflammation
Quercetin-associated change in surgery-associated marker of senescence
Secondary study objectives
Quercetin-dependent change in endothelium-dependent relaxation
Quercetin-dependent change in senescent arterial wall cell load
Quercetin-dependent change in senescent endothelial cell load
Other study objectives
Health status at follow-up visit.

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: QuercetinActive Control1 Intervention
Patients receiving 500 mg quercetin twice daily
Group II: PlaceboPlacebo Group1 Intervention
Patients receiving placebo twice daily

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Coronary Artery Disease (CAD) often focus on reducing inflammation and preventing cellular aging (senescence), which are critical in managing the disease. Anti-inflammatory treatments, such as statins, work by lowering cholesterol levels and reducing inflammation in the arterial walls, thereby preventing plaque buildup and improving blood flow. Anti-senescence treatments aim to delay the aging of vascular cells, which can help maintain the integrity and function of blood vessels. Quercetin, a polyphenol, is being studied for its potential anti-inflammatory and anti-senescence effects, which could provide additional benefits in reducing the progression of CAD. These mechanisms are crucial for CAD patients as they help prevent heart attacks and improve overall cardiovascular health.
Effects of Quercetin on Cardiac Function in Pressure Overload and Postischemic Cardiac Injury in Rodents: a Systematic Review and Meta-Analysis.Cardioprotective effects of quercetin against ischemia-reperfusion injury are age-dependent.Polyphenols: Potential source of drugs for the treatment of ischaemic heart disease.

Find a Location

Who is running the clinical trial?

Montreal Heart InstituteLead Sponsor
123 Previous Clinical Trials
80,660 Total Patients Enrolled
21 Trials studying Coronary Artery Disease
13,791 Patients Enrolled for Coronary Artery Disease
Michel Carrier, MDPrincipal InvestigatorMontreal Heart Institute
1 Previous Clinical Trials
3,000 Total Patients Enrolled

Media Library

Quercetin (Flavonoid) Clinical Trial Eligibility Overview. Trial Name: NCT04907253 — Phase 2
Coronary Artery Disease Research Study Groups: Quercetin, Placebo
Coronary Artery Disease Clinical Trial 2023: Quercetin Highlights & Side Effects. Trial Name: NCT04907253 — Phase 2
Quercetin (Flavonoid) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04907253 — Phase 2
~23 spots leftby Nov 2025