Clinical Trials in Brazil / NCT06169241
Recruiting Phase EARLY_PHASE1

Effect of Nitrate Supplementation on Blood Pressure and Microvascular Function of Resistant Hypertensive Patients

NCT06169241 · tracked via the Priya Life Science Brazil tracker
Phase
Phase EARLY_PHASE1
Started
2023-11-01
Last updated
2026-04-13

Condition(s) studied

Arterial HypertensionResistant HypertensionMicrovascular FunctionNitrate Supplementation

Investigational drug(s) / intervention(s)

Beetroot extractPlacebo

Beetroot extract: Beetroot extract powder supplementation with 400mg of nitrate per dose in the amount of 10g per day orally will be used in the group.

Placebo: The placebo will be administered as a colored and flavored isocaloric supplement composed of maltodextrin.

Study summary

Arterial hypertension (AH) has been identified as an important public health problem and considered a new epidemic with high mortality and morbidity. High blood pressure (BP) levels increase the chances of coronary artery disease (CAD), heart failure (HF), stroke, chronic renal failure (CRF) and death. Beetroot powder may be an easier way to increase the availability of nitric oxide and consequently vasodilation in these patients. However, studies are needed to evaluate its benefits in patients with AH.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Resistant hypertension, with a diagnosis described in the medical record, without changing medications or increasing doses in the last 30 days. Exclusion Criteria: * neoplasms * heart failure * use of medications with nitrate in their formula * patients undergoing renal denervation

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National Institute of Cardiology Rio de Janeiro Brazil Recruiting

More National Institute of Cardiology, Laranjeiras, Brazil trials in Brazil

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06169241 on ClinicalTrials.gov ↗ ← All trials in Brazil