Actively Recruiting

Phase Not Applicable
Age: 40Years - 65Years
All Genders
Healthy Volunteers
NCT06505967

Effectiveness of Qualia NAD+ Supplementation on Intracellular NAD Levels

Led by Qualia Life Sciences · Updated on 2024-07-17

200

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to determine if Qualia NAD+ effectively increases NAD+ levels in the blood and to evaluate its safety. Researchers will compare Qualia NAD+ to a placebo (a look-alike substance that contains no active drug) to assess its efficacy in increasing NAD+ levels in the blood. Participants will: Take Qualia NAD+ or a placebo every day for 4 weeks. Undergo blood tests before and after the trial.

CONDITIONS

Official Title

Effectiveness of Qualia NAD+ Supplementation on Intracellular NAD Levels

Who Can Participate

Age: 40Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Provide voluntary, written, informed consent to participate in the study
  • Agree to provide a valid cell phone number and receive communications through text
  • Healthy males and females aged 40 to 65 years
  • Willing to complete study questionnaires, records, and diaries
  • Willing to avoid supplements or products containing vitamin B3 starting 2 weeks before baseline and during the study
  • Willing to continue any current supplements except vitamin B3 during the study
  • Willing to self-administer the NAD fingerstick test at home for baseline and post-intervention samples
  • Willing to sign a release form allowing researchers access to test results
Not Eligible

You will not qualify if you...

  • Women who are pregnant, breastfeeding, or planning pregnancy during the trial
  • Known food intolerances or allergies to any product ingredients
  • Having psychiatric, neurologic, endocrine disorders, or cancer
  • History of a significant cardiovascular event within the past 6 months
  • Taking MAO inhibitors, SSRIs, or other psychiatric or neurological medications
  • Receiving immunosuppressive therapy
  • Adults without capacity to consent
  • Individuals incompatible with the test protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Qualia Life Sciences

Carlsbad, California, United States, 92011

Actively Recruiting

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Research Team

W

William Scuba

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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Effectiveness of Qualia NAD+ Supplementation on Intracellular NAD Levels | DecenTrialz