Prospective Human Study Evaluating Changes in Markers of Detoxification, Overall Physical and Mental Health, and Fatigue Following Supplementation With CellCore Protocols

Part of paid clinical trials in Richmond, Virginia.

Sponsor
OvationLab
Study ID
NCT07753798
Status
Not Yet Recruiting

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Conditions

  • Environmental Toxins
  • General Health

Eligibility Criteria

Sex
ALL
Age
25 Years - 65 Years
Healthy Volunteers
Not accepted

Interventions

  • CellCore Foundational Protocol — DIETARY_SUPPLEMENT
    The CellCore Foundational Protocol is a four-phase, four-month supplement program designed to support drainage, gut and immune balance, whole-body immune support, and systemic detoxification in a stepwise sequence.
  • CellCore - BioToxin Binder & Drainage Activator — DIETARY_SUPPLEMENT
    BioToxin Binder is a first-step detox support supplement that uses CellCore BioActive Carbon® carbon technology to bind biotoxins while supporting gut microbiome balance, immunity, digestive function, cellular repair, and energy production. Drainage Activator is a drainage-support supplement aimed at the extracellular matrix and lymphatic drainage, using herbs and mushrooms to help open drainage pathways and support the body's natural detox processes. This is a three-month combination protocol.

Study Details

The primary purpose of this study is to evaluate the effects of CellCore protocols on environmental toxicant biomarkers among adult patients with high baseline toxicant levels. Patients will be allocated to one of two CellCore protocols (Foundational Protocol or BioToxin Binder/Drainage Activator) based on overall physical health, mental health, and fatigue levels at baseline. A prospective, practitioner-led, open-label, single-arm intervention with the CellCore protocols will be conducted to measure pre- and post-intervention changes in urinary environmental toxicant biomarkers and validated, patient-reported health outcomes.

Key Dates

First listed
Aug 10, 2026
Start date
Aug 31, 2026
Status verified
Aug 2026
Primary completion
Jun 30, 2027
Completion
Jun 30, 2027

Study Design

Enrollment
40 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER

Arms

  • Experimental: CellCore - Foundational Protocol
  • Experimental: CellCore - BioToxin Binder + Drainage Activator

Primary Outcome Measure

Mosaic Envirotox Burden + Heavy Metals Urinary Panel [ Time Frame: Measured at baseline, one month, and end of protocol (4 months for Foundational Protocol & 3 months for BioToxin Binder + Drainage Activator protocol) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
OvationLabRichmondVirginia23220
Study Administration
[email protected]
‪(240) 232-2103‬

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By research site
OvationLab· Richmond, VA

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