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RECRUITING
NCT07285109
NA

The Impact of Qualia Vitamin C+ on Blood Vitamin C Levels

Sponsor: Qualia Life Sciences

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

25 Years - Any

Study Type

INTERVENTIONAL

Enrollment

36

Start Date

2025-12-22

Completion Date

2026-02-11

Last Updated

2025-12-16

Healthy Volunteers

Yes

Interventions

DIETARY_SUPPLEMENT

Qualia Vitamin C+

Qualia Vitamin C+ manufactured by Qualia Life Sciences

DIETARY_SUPPLEMENT

Placebo

Rice flour

Locations (1)

Qualia Life Sciences

Carlsbad, California, United States