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Study identifier: NCT06128278 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Acute Equol Supplementation and Vascular Function in Women With and Without CKD

Condition: Chronic Kidney Diseases · Vascular Function · Women  ·  Sponsor: University of Colorado, Denver

PhasePhase 2
Planned participants38
Who can joinFemale, 50 Years to 69 Years
Healthy volunteersYes

About this study

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 acute effect (1-hour, 2-hours, and 3-hours post ingestion) of oral equol supplementation on vascular function in postmenopausal women with and without CKD.

This description comes directly from the study's public registry record.

Talk to the study team

Ester Oh  ·  303-724-3765  ·  ester.oh@cuanschutz.edu

Emily Andrews  ·  303-724-7790  ·  taylor.struemph@cuanschutz.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Colorado Anschutz Medical CampusAurora, Colorado, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06128278