Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07428889

Nicotinamide Adenine Dinucleotide Responses to a Nutritional Supplement

A Randomized, Controlled, Pilot Trial to Assess the Effects of a Proprietary Nutritional Supplement on Nicotinamide Adenine Dinucleotide (NAD+) Responses in Healthy Adults

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
34 (estimated)
Sponsor
Shaklee Corporation · Industry
Sex
All
Age
45 Years – 65 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to evaluate nicotinamide adenine dinucleotide (NAD+) in response to a proprietary nutritional supplement in generally healthy adults, compared to placebo.

Detailed description

The objective of this study is to evaluate nicotinamide adenine dinucleotide (NAD+), its metabolites, and markers of health in response to a proprietary nutritional supplement in generally healthy adults, compared to placebo.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTProprietary Nutritional Supplement1000 mg nicotinamide metabolites and plant extracts, taken orally, daily for 60 days
DIETARY_SUPPLEMENTPlacebo Supplement1000 mg maltodextrin, taken orally, daily for 60 days

Timeline

Start date
2026-02-17
Primary completion
2026-06-01
Completion
2026-06-01
First posted
2026-02-24
Last updated
2026-04-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07428889. Inclusion in this directory is not an endorsement.