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IV Administration of ChromaDex's Niagen® as Compared to NAD+
NCT06382688 · View on ClinicalTrials.gov ↗
Study Summary
This is a 2-part study evaluating the effects of IV administration of NR on healthy adult populations. Study 1 involved all four arms with 37 people. The second study only included the active NR and NAD+ arms to further evaluate tolerability and comfort of the IV.
Conditions Studied
Interventions
- OTHER Placebo
- DIETARY_SUPPLEMENT NAD+ (nicotinamide adenine dinucleotide) IV
- DIETARY_SUPPLEMENT Niagen® (nicotinamide riboside) IV
- DIETARY_SUPPLEMENT Niagen® (nicotinamide riboside) oral
Study Locations (1)
Tennessee
- Nutraceuticals Research Institute — Franklin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 53 participants |
| Start Date | 2023-11-13 |
| Est. Completion | 2024-08-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06382688
The ClinicalTrials.gov registry entry for NCT06382688 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 53 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Nutraceuticals Research Institute, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Healthy Aging appearing as the primary indexed condition, and to 4 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06382688 reports 1 study location spanning 1 distinct geographic area — top geographies include Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06382688 about?
NCT06382688 is a clinical study titled "IV Administration of ChromaDex's Niagen® as Compared to NAD+". This is a 2-part study evaluating the effects of IV administration of NR on healthy adult populations. Study 1 involved all four arms with 37 people. The second study only included the active NR and NAD+ arms to further evaluate tolerability and comfort of the IV.
What is the current status of trial NCT06382688?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 53 participants. The study started on 2023-11-13. Estimated completion is 2024-08-31.
What conditions does trial NCT06382688 study?
This clinical trial studies the following conditions: Healthy Aging. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06382688?
The interventions under investigation include: Placebo (OTHER), NAD+ (nicotinamide adenine dinucleotide) IV (DIETARY_SUPPLEMENT), Niagen® (nicotinamide riboside) IV (DIETARY_SUPPLEMENT), Niagen® (nicotinamide riboside) oral (DIETARY_SUPPLEMENT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06382688?
This trial is sponsored by Nutraceuticals Research Institute, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06382688 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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