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Pharmacokinetics of Berkeley Life Oral Nitrate Supplementation

NCT06777108 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2025-01-17

No results posted yet for this study

Summary

The purpose of the study is to examine the way that a nitric oxide supplement moves through the body. Specifically, the relationship between saliva and blood concentration of the supplement and the elapsed time since taking the supplement.

Participants will :

* Come to UVA to participate in testing procedures.
* Take a nitric oxide supplement up to twice.
* Complete a pregnancy test if the participant is a pre-menopausal female.
* Produce saliva into a tube to collect a sample.
* Undergo several blood draws (less than 6 tablespoons).
* Wear a 24-hour non-invasive device that monitors the participant's blood pressure.

Conditions

Interventions

DIETARY_SUPPLEMENT

Inorganic Nitrate

The intervention evaluates the single and 1/2-dose pharmacokinetics of a plant-based bioequivalent inorganic nitrate (NO3-) complex with vitamins, antioxidantsand phytophenol rich food extracts.

Sponsors & Collaborators

  • University of Virginia

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-07
Primary Completion
2024-04-06
Completion
2024-04-06

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06777108 on ClinicalTrials.gov