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RECRUITING
NCT06128278
PHASE2

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

Sponsor: University of Colorado, Denver

View on ClinicalTrials.gov

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 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.

Official title: Acute Equol Supplementation and Vascular Function in Postmenopausal Women With and Without CKD

Key Details

Gender

FEMALE

Age Range

50 Years - 69 Years

Study Type

INTERVENTIONAL

Enrollment

38

Start Date

2023-03-07

Completion Date

2026-12-31

Last Updated

2025-09-30

Healthy Volunteers

Yes

Interventions

DRUG

S-equol

Oral supplementation of S-equol

OTHER

Placebo

Oral supplementation of placebo

Locations (1)

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States