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Salt; Excess clinical trials

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NCT ID: NCT03753204 Recruiting - Inflammation Clinical Trials

Salt-Sensitivity and Immunity Cell Activation

Start date: September 1, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

Salt-sensitive hypertension affects nearly 50% of the hypertensive and 25% of the normotensive population, and strong evidence indicates that reducing salt intake decreases blood pressure and cardiovascular events. The precise mechanisms of how dietary salt contributes to blood pressure elevation, renal injury, and cardiovascular disease remains unclear. Our data indicated that monocytes exhibit salt sensitivity, and the investigators hypothesize that of salt sensitivity of these and similar immune cells correlate with the hypertensive response to salt intake. Currently, the research tools for diagnosing salt-sensitivity are costly, time consuming and laborious. In this study the investigators will identify monocyte salt-sensitivity as a marker of salt-sensitive hypertension.

NCT ID: NCT03696433 Completed - Obesity Clinical Trials

Visualizing Vascular Mechanisms of Salt Sensitivity

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

This study aims to assess the salt sensitive blood pressure response to dietary salt load compared with radiological markers of salt handling.

NCT ID: NCT02727426 Recruiting - Salt; Excess Clinical Trials

Dietary Salt and Microvascular Function

Start date: February 2016
Phase: N/A
Study type: Interventional

It is well accepted that high-salt (HS) intake is an essential risk factor in development and progression of hypertension. Results of some recent studies suggest that some of the deleterious effects of a HS diet are independent of elevated blood pressure (BP) and may occur in normotensive individuals and are associated with impaired endothelial function. However, the effects of acute salt loading on endothelial function and vascular reactivity in young healthy individuals are still scarce and inconsistent. The purpose of present study is to determine whether one week of HS intake affects microvascular reactivity in young healthy subjects without changes in BP. In addition, the investigators sought to evaluate if potential HS diet-induced microvascular dysfunction is associated with changes in oxidative stress level and/or with modification of immunological response in young healthy subjects.