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Not Yet RecruitingNCT07132801

Comparison of Two Qualia NAD⁺ Formulations on Intracellular NAD⁺ Levels

Comparison of Two Qualia NAD⁺ Formulations on Intracellular NAD⁺ Levels: A Randomized, Double-Blind, Placebo-Controlled Three-Arm Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
180 (estimated)
Sponsor
Qualia Life Sciences · Industry
Sex
All
Age
35 Years – 75 Years
Healthy volunteers
Accepted

Summary

This is a randomized, double-blind, placebo-controlled, parallel-group study evaluating the effects of two distinct Qualia NAD⁺ formulations on intracellular NAD⁺ levels in healthy adults aged 35-75 years. Approximately 180 participants will be randomized to one of three study arms: Qualia NAD⁺ version 1, Qualia NAD⁺ version 2, or placebo. Each participant will take two capsules of their assigned product once daily in the morning, with or without food, over a 28-day period. The primary outcome is the change in intracellular NAD⁺ levels, assessed via at-home finger-stick blood collection at baseline and study completion. Secondary endpoints include changes in aging-related symptoms (AMFS scores), health-related quality of life (RAND SF-36), and evaluation of safety and tolerability. All assessments, including electronic questionnaires, are completed remotely without in-person visits.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTQualia NAD⁺ version 1Qualia NAD+ version 1 manufactured by Qualia Life Sciences
DIETARY_SUPPLEMENTQualia NAD⁺ version 2Qualia NAD+ version 2 manufactured by Qualia Life Sciences
DIETARY_SUPPLEMENTPlaceboRice Flour

Timeline

Start date
2025-10-13
Primary completion
2025-11-30
Completion
2025-12-15
First posted
2025-08-20
Last updated
2025-08-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07132801. Inclusion in this directory is not an endorsement.