See if CellCore protocols change environmental toxin biomarkers and health in adults

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 prospective, open-label, single-arm study assigns adults with elevated urinary environmental toxicants to either the Foundational Protocol or the BioToxin Binder/Drainage Activator based on baseline health and fatigue. The trial measures changes in urinary toxicant biomarkers and patient-reported health outcomes before and after the intervention. Participants must be under the care of a qualified practitioner, live in the United States, and complete testing and questionnaires. The study is led by OvationLab in Richmond, VA, with no listed collaborators.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Adult between 25 and 65 years of age
2. Documented elevated urinary environmental toxicant levels above the 75th percentile of at least 5 toxins on baseline environmental toxin test
3. PROMIS - Global Health - Physical Health t-scores \< 42.4 for Foundational Protocol (otherwise BioToxin Binder/Drainage Activator Protocol)
4. Currently receiving care from a qualified, participating practitioner
5. Lives in the United States
6. Ability to speak and read English
7. Willing and able to follow the assigned CellCore protocols and complete all required testing and questionnaires
8. Willing and able to provide informed consent

Exclusion Criteria:

1. Currently undergoing active chelation therapy
2. Participation in a structured detoxification program within the prior 60 days, including use of activated charcoal, bentonite/zeolite clay, chlorella, cholestyramine
3. Ongoing occupational toxic exposure (e.g., working on golf course, dry cleaning facility) that cannot be reduced or controlled during the study period
4. Pregnancy or lactation, or planning pregnancy during the study period
5. Major comorbid medical condition requiring complex specialty management that, in the practitioners' clinical judgment, would interfere with safe study participation
6. Anticipated initiation of additional detoxification products, major dietary changes, or other significant co-interventions during the study period
7. Unable or unwilling to provide informed consent

Where it's running

• OvationLab
  Richmond, Virginia, United States Recruiting

Study contacts

• Study coordinator: Study Administrator
• Email: info@ovationlab.com
• Phone: ‪(240) 232-2103‬

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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.