Clinical Trials Directory

Trials / Completed

CompletedNCT03707652

Open-label Study to Assess Increasing Levels of NAD+(Nicotinamide Adenine Dinucleotide)

Three-Day Dosing NAD + Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Supplement Formulators, Inc. · Industry
Sex
All
Age
30 Years – 80 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to assess an effective single oral supplement or combination of oral supplements for increasing whole blood NAD+ levels.

Detailed description

This is a open-label dose finding study to detect an effective single oral supplement or combination of oral supplements for enhancing whole blood levels of NAD+. Each subject will receive a specific dose of the formulation once daily for 3 days followed by a washout period. Upon completion of the treatment phase, there is a post-treatment period of assessments. Participants receive assessments of blood tests, vital signs, body weight with completion of questionnaires. The primary objective of the study is to identify the ideal dosage of an oral supplement to increase whole blood NAD+ levels in adults. The secondary objective of the study is to monitor for safety from a change in fasting blood chemistry panel parameters after three day's dosing compared to cycle baseline.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTOral supplement A1, 2 or 4 capsules daily of oral supplement A for 3 days
DIETARY_SUPPLEMENTOral supplement B4 capsules daily of oral supplement B for 3 days
DIETARY_SUPPLEMENTOral supplement C1,2 or 4 capsules daily of oral supplement C for 3 days
DIETARY_SUPPLEMENTOral supplement D1 or 2 tablets daily of oral supplement D for 3 days
DIETARY_SUPPLEMENTOral Supplement D in combination with oral supplement C1 or 2 tablets of oral supplement D in combination with 2 or 4 capsules of oral supplement C for 3 days

Timeline

Start date
2018-03-12
Primary completion
2018-05-16
Completion
2018-05-24
First posted
2018-10-16
Last updated
2018-10-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03707652. Inclusion in this directory is not an endorsement.