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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04101188
Other study ID # 1472577
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 16, 2020
Est. completion date December 31, 2024

Study information

Verified date May 2023
Source University of Delaware
Contact Liza J Walker, BS
Phone (302)831-3181
Email lizaj@udel.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Americans continue to consume high amounts of sodium. Potassium is notable for its blood pressure lowering effects but less is known regarding its effect on the vasculature. This investigation seeks to determine the role of dietary potassium on the vasculature in the presence of a high sodium diet in salt-resistant adults.


Description:

Significant public health efforts have been made towards salt reduction but most have met with failure. Dietary factors such high sodium/low potassium diets contribute to the development of cardiovascular diseases (CVDs) such as atherosclerosis and high blood pressure (BP). This is important as CVD is the number one killer in the U.S. While the role of these two nutrients on BP is widely accepted, their impact on the vasculature has received less attention. Endothelial dysfunction, characterized by impaired dilation, is an important non-traditional risk factor for atherosclerosis. Evidence supporting potassium's beneficial role on vascular health remains unclear although it may be more effective in the presence of a high sodium diet. A purported mechanism responsible for sodium-induced vascular dysfunction is overproduction of reactive oxygen species (ROS) resulting in reduced nitric oxide (NO) production/bioavailability. Additionally, high sodium diets have been shown to stiffen the endothelium. This investigation will evaluate the vascular effects of dietary potassium during a high salt diet including its impact on sodium-induced oxidative stress and endothelial cell stiffness.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date December 31, 2024
Est. primary completion date August 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - healthy - normal blood pressure - normal resting ECG Exclusion Criteria: - hypertension - history of heart disease - diabetes - kidney disease - obese (BMI =30) - significant weight changes in the last 6 months - use of tobacco products - pregnant - on a special diet (gluten free; vegan) - take any medications for the above conditions - endurance trained athletes

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Moderate Potassium/Low Sodium Diet
Consumption of 10 days of a diet moderate in potassium and low in sodium.
Moderate Potassium/High Sodium Diet
Consumption of 10 days of a diet moderate in potassium and high in sodium.
High Potassium/High Sodium Diet
Consumption of 10 days of a diet high in potassium and high in sodium.

Locations

Country Name City State
United States University of Delaware Newark Delaware

Sponsors (1)

Lead Sponsor Collaborator
University of Delaware

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Conduit artery endothelial-dependent dilation The change in flow-mediated dilation (FMD) between the 3 diets as assessed by brachial artery FMD on day 10 of the diet
Primary Microvascular function Cutaneous microvascular dilatory response to local heating assessed by laser Doppler flowmetry coupled with intradermal microdialysis on day 10 of the diet
Secondary Ambulatory BP monitoring assessed by 24-hour ambulatory blood pressure on day 7 and 10 of diet
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