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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03943459
Other study ID # 408720/2018-2
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date August 2, 2019
Est. completion date June 30, 2022

Study information

Verified date October 2019
Source InCor Heart Institute
Contact Antonio P Mansur, PhD
Phone +551126615387
Email apmansur@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Higher consumption of fruits and vegetables promote greater availability of phenolic compounds and these compounds were associated with vascular health. Quercetin, a phenolic compound, is the most abundant natural antioxidant belonging to the group of flavonoids. Quercetin improved lipoprotein metabolism, had antioxidant capacity, produced vasodilating substances in the vascular endothelium and reduced platelet aggregability. Likewise, statins are medications known to reduce cardiovascular events in women with coronary disease by reducing serum LDL-cholesterol. Therefore, a number of metabolic pathways are responsible for vascular health. The serum concentration and gene expression of sirtuin 1 (Sirt1) and RAGE soluble (sRAGE) are directly associated with vascular protection. This study will analyse the influence of atorvastatin and quercetin on serum concentrations and gene expression of Sirt1 and sRAGE in postmenopausal women with stable coronary artery disease.


Description:

Higher consumption of fruits and vegetables promote greater availability of phenolic compounds and these compounds were associated with vascular health. Quercetin, a phenolic compound, is the most abundant natural antioxidant belonging to the group of flavonoids. Quercetin improved lipoprotein metabolism, had antioxidant capacity, produced vasodilating substances in the vascular endothelium and reduced platelet aggregability. Likewise, statins are medications known to reduce cardiovascular events in women with coronary artery disease (CAD) by reducing serum LDL-cholesterol. Therefore, a number of metabolic pathways are responsible for vascular health. The serum concentration and gene expression of sirtuin 1 (Sirt1) and RAGE soluble (sRAGE) are directly associated with vascular protection. This study will analyse the influence of atorvastatin and quercetin on serum concentrations and gene expression of Sirt1 and sRAGE in postmenopausal women with stable coronary artery disease and also the correlation between the changes in serum concentration of Sirt1 and sRAGE and the changes in lipid profile, inflammatory biomarkers and sex hormones in response to these drugs. This is a 60-day randomized, double blind, placebo-controlled study in 60 postmenopausal women with CAD, divided into three groups with 20 women each: Group 1 - Quercetin (500 mg / day); Group 2 - atorvastatin (80 mg / day): Group 3 - control.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 30, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers No
Gender Female
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- postmenopausal women,

- angiographic documented coronary artery disease,

- stable coronary artery disease

Exclusion Criteria:

- BMI <18,1 Kg/m2,

- smoking,

- hypo or hyperthyroidism,

- rheumatic disease,

- use of alcohol,

- hepatic failure,

- renal failure

- hormone replacement therapy

- use of insulin

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Quercetin
Quercetin 250 mg BID

Locations

Country Name City State
Brazil INCOR - Heart Institute São Paulo

Sponsors (1)

Lead Sponsor Collaborator
InCor Heart Institute

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sirtuin-1 serum concentration of sirtuin-1 60 days
Primary Soluble receptor for advanced glycation end products serum concentration of soluble receptor for advanced glycation end products 60 days
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