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Effect of a Dietary Supplement Versus Placebo on Serum PFAS Levels in Male Firefighters

RecruitingHealthy volunteers welcome

A Randomized, Double-Blind, Placebo-Controlled, Cross-Over Pilot Study Evaluating a Dietary Supplement Supporting Natural Elimination Processes in Male Firefighters

Who can join

Ages 18 and older · Men · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* Able to give written informed consent
* Male firefighter with previous career exposure to PFAS
* BMI between 18.5 and 35 kg/m²
* Serum PFOS level ≥5 ng/mL at screening
* Willing to consume the study product daily for the duration of the study

Exclusion Criteria:

* History of drug and/or alcohol abuse (\>15 standard drinks per week)
* Food allergy, intolerance or dietary restriction that, in the opinion of the investigator, would preclude consumption of the study product
* Blood donation within the past 3 months
* Current smoker of \>20 cigarettes per day, or former smoker with a history of ≥20 cigarettes per day who quit within 6 months prior to Visit 1
* Any significant acute or chronic health condition that would prevent participation, pose a risk, or confound interpretation of results, including: diagnosed gastrointestinal disorders (irritable bowel syndrome, inflammatory bowel disease, Crohn's disease, ulcerative colitis, coeliac disease, or other chronic diarrhoeal disorders); uncontrolled medical conditions; history of chronic kidney or liver disease; chronic inflammatory or autoimmune disease; history of gastrointestinal surgery; hospitalisation within the past 3 months
* Current or recent (past 12 weeks) use of medications affecting bile acid metabolism (e.g. bile acid sequestrants, fibrates) or antibiotics
* Current or recent (past 4 weeks) use of supplements affecting gut microbiota (prebiotics, probiotics, postbiotics, fibres, synbiotics), detoxification pathways (milk thistle, N-acetylcysteine, glutathione) or bile acid metabolism (e.g. psyllium husk)
* Current or recent (past 2 weeks) consumption of prohibited foods, including probiotic yoghurts
* Considered by the investigator unlikely to comply with study requirements
* Current participation in another clinical study, or insufficient time elapsed since a previous experimental study

About the study

This study is designed to evaluate the effect of a probiotic dietary supplement containing Streptococcus salivarius on serum PFAS levels in male firefighters with documented occupational PFAS exposure, following twice-daily use over a 12-week period.

What is being tested

Sponsor: Cambiotics ApS · Participants: 70 · Started: Oct 8, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07846371

Locations in the U.S.

IllinoisAtlantia Clinical Trials, Chicago

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.