Fulvic acid supplements for metabolic syndrome

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study will compare two doses of fulvic acid to placebo over 12 weeks in adults with metabolic syndrome or prediabetes. Participants will receive either 50 mg or 100 mg of fulvic acid daily, or a placebo, to see if the supplement improves metabolic markers and related symptoms. The trial builds on limited prior work and aims to provide controlled data on safety and efficacy in this population. Recruitment is planned at a site in Phoenix, Arizona under the lead sponsorship of Arizona State University. Outcomes will focus on metabolic parameters and markers of metabolic health.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* metabolic syndrome or prediabetes

Exclusion Criteria:

* pregnant or nursing
* multiple medications to treat obesity, heart disease, thyroid conditions, cancer
* smokers
* competing athletes
* vegetarians

Where it's running

• PBC 850 N 5th Street
  Phoenix, Arizona, United States Recruiting

Study contacts

• Study coordinator: Carol Johnston, PhD
• Email: carol.johnston@asu.edu
• Phone: 6024963463

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.