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Trials / Completed

CompletedNCT04223531

The Natriuretic Peptide Response to Saline Infusion

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Vanderbilt University Medical Center · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The primary objective is to evaluate the overarching hypothesis that obese and black individuals have relatively lower circulating natriuretic peptide levels compared with lean and white individuals. Conventional clinical assays for measurement of circulating natriuretic peptides display substantial overlap, precluding determination of the basis of the relative natriuretic peptide deficiency previously observed in these groups. We will study lean or obese, black or white, healthy adult subjects with intravenous (IV) saline infusion as a stimulus for natriuretic peptide production and release. We will measure circulating levels of natriuretic peptide isoforms using mass spectrometry that allows the specific identification of proBNP 1-108 and its cleavage product BNP 1-32.

Conditions

Interventions

TypeNameDescription
DRUGNormal Saline 0.9% Infusion Solution BagParticipants will receive a normal saline infusion at a rate of 10ml per unit of body surface area per minute for 120 minutes.

Timeline

Start date
2020-10-26
Primary completion
2022-06-17
Completion
2022-06-17
First posted
2020-01-10
Last updated
2023-01-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04223531. Inclusion in this directory is not an endorsement.

The Natriuretic Peptide Response to Saline Infusion (NCT04223531) · Clinical Trials Directory