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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03501433
Other study ID # 17-603
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2018
Est. completion date December 1, 2019

Study information

Verified date September 2020
Source Iowa State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effects of Nicotinamide Riboside (NR) supplementation on metabolism and vascular function following high-fat meal. Differences between young (18-35) and older (60-75) adults will be determined.


Description:

The purpose of this study is to determine the effects of 7 days of Nicotinamide Riboside (NR) or placebo supplementation on metabolism and vascular function following high-fat meal. Differences between young (18-35) and older (60-75) adults will be determined.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date December 1, 2019
Est. primary completion date December 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Age 18 to 35 (young) and 60 to 75 (older)

- Normo- or pre-hypertensive (blood pressure <140/90 mmHg)

- Non-smokers

- Able to give informed consent and participate in all laboratory visits

Exclusion Criteria:

- Currently taking any medications that could interfere with cardiovascular or metabolic outcomes will be excluded from the study (e.g., beta-blockers)

- Known metabolic (e.g. Type I or Type II diabetes, cardiovascular disease, etc.) or immunologic (e.g. HIV, cancer, autoimmune, etc.) diseases

- Food allergies to egg, milk, soy or wheat

- Women who are pregnant or planning to become pregnant during the course of the study,

- Pacemaker or other implanted device

- Unwilling to participate in the experimental protocol or blood draws will be excluded

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Nicotinamide riboside chloride (Niagen)
250 mg capsules 2x/day for 7 days
Placebo
2x/day for 7 days

Locations

Country Name City State
United States Iowa State University Ames Iowa

Sponsors (1)

Lead Sponsor Collaborator
Iowa State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary NAD+ Blood and peripheral blood mononuclear cell (PBMC) levels 7 days
Secondary Vasodilatory responsiveness Post-Occlusion Reactive Hyperemia (PORH) 7 days
Secondary Lipdemia Fasting and postprandial 7 days
Secondary Oxidative stress and inflammation Plasma markers and expression in circulating PBMCs 7 days
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