Effectiveness of Qualia Testosterone Supplementation on Testosterone Levels

Part of paid clinical trials in Carlsbad, California.

Sponsor
Qualia Life Sciences
Study ID
NCT07028255
Status
Not Yet Recruiting

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Conditions

  • Testosterone

Eligibility Criteria

Sex
MALE
Age
28 Years - 65 Years
Healthy Volunteers
Accepted

Interventions

  • Qualia Testosterone — DIETARY_SUPPLEMENT
    Qualia Testosterone manufactured by Qualia Life Sciences
  • Placebo — DIETARY_SUPPLEMENT
    Rice Flour

Study Details

This is a randomized, double-blind, placebo-controlled parallel trial designed to assess the efficacy of Qualia Testosterone, a novel dietary supplement, in adult males aged 28 to 65 experiencing symptoms associated with testosterone deficiency. Approximately 60 participants will be randomized to receive either Qualia Testosterone (2 capsules daily) or a matched placebo for 21 days, with dosing administered each morning. The study's primary outcomes are changes in total testosterone, free testosterone (via dialysis), and dihydrotestosterone levels from baseline to Week 3. Secondary outcomes include changes in Aging Male Symptoms Scale scores-encompassing psychological, somatic, and sexual domains-as well as safety and tolerability. Blood samples will be collected in a laboratory setting, while symptom and safety assessments will be completed electronically at home.

Key Dates

Start date
Jul 1, 2025
Status verified
Jun 2025
Primary completion
Sep 1, 2025
Completion
Oct 1, 2025

Study Design

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

Arms

  • Active Comparator: Qualia Testosterone
    Qualia Testosterone manufactured by Qualia Life Sciences
  • Placebo Comparator: Placebo
    Rice Flour

Primary Outcome Measure

Between-group change in blood testosterone levels [ Time Frame: 3 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Qualia Life SciencesCarlsbadCalifornia92011
Abhi Ardagh
855-281-2328

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