RecruitingPhase 2NCT07194590

Equol and Vascular Function in Women With Chronic Kidney Disease

Equol Supplementation for Improving Vascular Function in Postmenopausal Women With CKD


Sponsor

University of Colorado, Denver

Enrollment

74 participants

Start Date

Feb 19, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The risk of cardiovascular disease (CVD) is significantly elevated in patients with chronic kidney disease (CKD). Notably, women with CKD commonly experience menstrual disturbances induced by CKD, which may contribute to impaired vascular function and elevated CVD risk. However, most of the literature in nephrology focuses on male patients, and studies on women's vascular health are limited. Establishing effective therapies for improving vascular function and reducing CVD risk in women with CKD is a high research priority of the NIH. Equol contributes to improvement in vascular function, mediated in part by its anti-oxidative and anti-inflammatory properties. However, there is no information on the effect of equol on vascular function in women with CKD. The proposed project aims to determine the effect of 12 weeks of oral equol supplementation on vascular function in postmenopausal women with CKD.


Eligibility

Sex: FEMALEMin Age: 50 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Equol and a drug called Placebo for people with blood pressure, cerebrovascular function, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGEquol

This group will receive 10 mg equol per day (2 capsules/day, 5mg equol/capsule).

DRUGPlacebo

This group will receive 2 placebo capsules per day.


Locations(1)

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States

View Full Details on ClinicalTrials.gov

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NCT07194590


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