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NCT07285109 · ClinicalTrials.gov registry record · NA
The Impact of Qualia Vitamin C+ on Blood Vitamin C Levels
A NA study of Vitamin C Deficiency, sponsored by Qualia Life Sciences.
- Recruiting
- Registry status
- NA
- Development phase
- 36
- Enrollment target
- 1
- Study location
NCT07285109 is a NA study of Vitamin C Deficiency that is actively recruiting participants, run by Qualia Life Sciences. The registered enrollment target is 36 participants. The trial reports 1 study location across 1 state.
The verdict
NCT07285109, a NA study of Vitamin C Deficiency, is actively recruiting participants, sponsored by Qualia Life Sciences.
- RECRUITING
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a randomized, double-blind, placebo-controlled, parallel-group, study evaluating the effect of a Qualia Vitamin C+ formulation on Whole Blood Vitamin C levels in the blood of healthy adults aged 25 years or older. Approximately 36 participants will be randomized to one of two study arms: Qualia Vitamin C+ 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 blood vitamin C levels, assessed via in lab blood collection at baseline and study completion. Secondary endpoints include questionnaires measuring health-related cognitive functioning and stress (PROMIS Cognitive Function - Short Form 8a and the Perceived Stress Scale-10), the Single-item Assessment of Immune Fitness, evaluation of safety and tolerability, and an Overall Experience Questionnaire (Appendices 1, 4-7). All assessments, including electronic questionnaires, are completed remotely without in-person visits.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Qualia Vitamin C+
Study Locations (1)
California
- Qualia Life Sciences - Carlsbad
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2025-12-22 |
| Est. Completion | 2026-02-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07285109
The ClinicalTrials.gov registry entry for NCT07285109 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Qualia Life Sciences, which has 10 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Vitamin C Deficiency appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT07285109 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT07285109 about?
NCT07285109 is a clinical study titled "The Impact of Qualia Vitamin C+ on Blood Vitamin C Levels". This is a randomized, double-blind, placebo-controlled, parallel-group, study evaluating the effect of a Qualia Vitamin C+ formulation on Whole Blood Vitamin C levels in the blood of healthy adults aged 25 years or older. Approximately 36 participants will be randomized to one of two study arms: Qua...
What is the current status of trial NCT07285109?
This trial is currently recruiting. It is a NA study. The enrollment target is 36 participants. The study started on 2025-12-22. Estimated completion is 2026-02-11.
What conditions does trial NCT07285109 study?
This clinical trial studies the following conditions: Vitamin C Deficiency.
What interventions are being tested in trial NCT07285109?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Qualia Vitamin C+ (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT07285109?
This trial is sponsored by Qualia Life Sciences, which has 10 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07285109 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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