Effectiveness of Qualia Magnesium+® Supplementation on RBC Magnesium Levels

Part of paid clinical trials in Carlsbad, California.

Sponsor
Qualia Life Sciences
Study ID
NCT06979648
Status
Not Yet Recruiting

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Conditions

  • Magnesium Deficiency

Eligibility Criteria

Sex
ALL
Age
21 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Qualia Magnesium+® — DIETARY_SUPPLEMENT
    Qualia Magnesium+® manufactured by Qualia Life Sciences
  • Placebo — DIETARY_SUPPLEMENT
    Rice Flour

Study Details

This is a randomized, double-blind, placebo-controlled parallel trial designed to evaluate the effectiveness of Qualia Magnesium+® supplementation on red blood cell (RBC) magnesium levels in adults aged 21 and older. Approximately 100 participants with baseline RBC magnesium levels below 6.0 mg/dL will be randomly assigned to receive either Qualia Magnesium+ or a placebo. Participants will take 2 capsules daily in the evening, with or without food, for a duration of 12 weeks. The primary outcome is the between-group change in RBC magnesium levels from baseline to Week 12. Secondary outcomes include assessments of sleep quality, perceived stress, magnesium status, and safety and tolerability. Data collection will occur through lab bloodwork and electronic questionnaires.

Key Dates

Start date
May 21, 2025
Status verified
May 2025
Primary completion
Aug 21, 2025
Completion
Sep 21, 2025

Study Design

Enrollment
100 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Active Comparator: Qualia Magnesium+®
    Qualia Magnesium+® Supplement
  • Placebo Comparator: Placebo
    Rice Flour

Primary Outcome Measure

Between-group change in RBC magnesium levels [ Time Frame: 12 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Qualia Life SciencesCarlsbadCalifornia92011
Abhi Argagh
[email protected]
855-281-2328

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By research site
Qualia Life Sciences· Carlsbad, CA