Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60
Sex
Women only
Ages
Ages 55 Years to 70 Years
Primary completion
2023-12-23
Last update
2025-12-19

What this trial studies

Chronic coronary syndrome (CCS) is the leading cause of death in women in the most developed regions of Brazil. The primary etiopathogenic mechanism is the process of atherosclerosis. A healthy diet rich in fruits and vegetables is associated with a lower incidence of CCS. The higher consumption of these foods promotes greater availability of phenolic compounds, and the higher intake of these compounds is one of the main hypotheses for vascular health.

Conditions in scope

  • Coronary Artery Disease
  • Menopause

Interventions

  • Quercetin (Dietary Supplement) — Trans-quercetin, 1000 mg daily for 60 days
  • Placebo (Dietary Supplement) — Starch, 1000 mg daily for 60 days

Who can join

Women only · Ages 55 Years to 70 Years

Inclusion criteria

  • Postmenopausal women;
  • Diagnosed coronary artery disease;
  • Stable coronary disease;

Exclusion criteria

  • hypo or hyperthyroidism,
  • rheumatic disease,
  • use of alcohol,
  • hepatic failure,
  • renal failure
  • hormone replacement therapy
  • use of insulin

Eligibility wording paraphrased from the public record. View the full criteria on ClinicalTrials.gov before contacting a site.

Where it’s happening

CityState / RegionFacilitySite status
São Paulo São Paulo INCOR- Heart Institute Unknown

Status & timeline

  • Overall status: Completed
  • Study type: Interventional
  • Phase: N/A
  • Start date: 2021-10-03
  • Primary completion: 2023-12-23
  • Last update posted: 2025-12-19
  • First posted: 2023-05-26

Lead sponsor: InCor Heart Institute (Other)

For trial site contact information, use the official record at ClinicalTrials.gov. Contact details change frequently and the public record is the source of truth.

Outcome measures

Primary outcomes

  • Estradiol (60 days)
    serum concentrations
  • Estrone (60 days)
    serum concentrations
  • Sirtuin-1 (60 days)
    Serum concentrations and gene expression

If you’re reading this trial because you have menopause symptoms now, you don’t have to wait for a trial to access evidence-based care. ClearedRx prescribes the same FDA-approved and compounded HRT products that have been studied in trials like this one for decades.

Important. Information from ClinicalTrials.gov as of May 8, 2026. Trial details (status, sites, contacts, eligibility, outcomes) change frequently — always check the official record at https://clinicaltrials.gov/study/NCT05877235 before contacting a site.

ClearedRx is not affiliated with this trial or its sponsor. We index public-domain ClinicalTrials.gov records to help patients find evidence-based context for menopause care decisions. ClearedRx itself is a telehealth menopause/HRT brand — we do not enroll patients in trials.