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ACTIVE NOT RECRUITING
NCT06584331
NA

BEETROOT JUICE INTAKE in POSTMENOPAUSAL HYPERTENSIVE WOMEN

Sponsor: Federal University of Uberlandia

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to verify the hemodynamic and biomarker responses of beetroot juice intake in postmenopausal women with hypertension. The main questions it aims to answer are: Is beetroot juice dose related to better hemodynamic responses in hypertensive postmenopausal women? Is beetroot juice dose related to better oxidative stress profile responses in hypertensive postmenopausal women? The investigators will conduct a parallel clinical study with 10 days of intervention, in which 48 women will be randomized into 3 groups: 1) Two shots of beetroot juice intake per day (800mg of NO3-); 2) One shot of beetroot juice intake per day (400mg of NO3-); 3) placebo intake (beetroot juice without NO3-).

Official title: HEMODYNAMIC and BIOCHEMICAL RESPONSES to 10 DAYS of BEETROOT JUICE INTAKE in POSTMENOPAUSAL HYPERTENSIVE WOMEN

Key Details

Gender

FEMALE

Age Range

45 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2024-08-07

Completion Date

2028-12

Last Updated

2024-09-23

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

1 dose of Beetroot juice intake

The volunteers will ingest 70 ml of beetroot juice with 400 mg of nitrate every morning for 10 days

DIETARY_SUPPLEMENT

2 doses of Beetroot juice intake

This group will ingest 2 shots of 70 ml of beetroot juice with 400mg of nitrate, in each shot, for 10 days.

DIETARY_SUPPLEMENT

Placebo

In this group, the participants will receive 70ml of low-nitrate beetroot juice to consume in the morning.

Locations (1)

FAEFI

Uberlândia, Minas Gerais, Brazil