Qualia Iron Formulations for Iron Deficiencies

This study is looking at how two different iron supplements, Qualia Iron Version A and Qualia Iron Version B, affect iron levels in the body compared to a placebo (a pill with no active ingredients, like rice powder). Researchers want to see if these supplements can improve iron status in healthy adults who may have iron deficiencies. They will measure changes in your iron levels over 8 weeks. About 40 adults aged 18 and older will participate. The current status of this study is unclear, so it's not known if they are actively recruiting.

Study design
This is a randomized, double-blind study, meaning participants are randomly assigned to a group and neither you nor the researchers will know which treatment you are receiving. Approximately 40 healthy adults will participate.
What's involved
You would take one or two capsules once daily for 56 days (8 weeks), following a schedule of 5 days on and 2 days off. You would also agree not to start new supplements during the study.
Compensation
Not stated in the trial record.
Follow-up
The study will assess changes in iron levels over 8 weeks, with measurements taken at 4 weeks and 8 weeks.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07156526

Impact of Two Iron Formulations on Iron Biomarkers and Quality of Life

Not Yet Recruiting
NAAges 18+Interventional
Qualia Life Sciences
~40 participants
Updated 2025-09-05 on ClinicalTrials.gov
What's tested:Qualia Iron Version AQualia Iron Version BPlacebo

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Changes in iron status biomarkers
Measured over From 0-4 weeks, 4-8 weeks, and 0-8 weeks
Iron Deficiencies

NCT07156526

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Qualia Life Sciences

    Carlsbad, Californiastudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • William Scuba · PRINCIPAL_INVESTIGATOR · Qualia Life Sciences

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Eligibility criteria

Inclusion

Provide voluntary, written, informed consent to participate in the study
Agree to provide a valid cell phone number and are willing to receive communications through text
Can read and write English
Willing to not begin taking any new supplements during the study and continue taking any supplements they are currently using regularly
Willing to complete questionnaires, records, and diaries associated with the study.
If the participant responded "Yes" to ≥2 questions on the custom Iron Inadequacy Questionnaire. Preference will be given to participants with a higher score.
If a participant has the following:

Exclusion

Women who are pregnant, breastfeeding, or planning to become pregnant during the trial
Known food intolerances/allergy to any ingredients in the product
Having any of the following conditions: Psychiatric conditions, neurologic disorders, endocrine disorders, irritable bowel disease, cancer
Having had a significant cardiovascular event in the past 6 months
Taking MAO inhibitors, SSRIs, or any other psychiatric or neurological medicines
On immunosuppressive therapy
Individuals who were deemed incompatible with the test protocol
Adults lacking capacity to consent
Individuals taking any of the following medications:
  • Changes in iron status biomarkersFrom 0-4 weeks, 4-8 weeks, and 0-8 weeks

    Between-groups changes in ferritin levels (ng/mL) will be assessed.