Effects of Probiotic Oral Intake on Plasma Chlordecone (Kepone) Concentrations in Individuals Environmentally Exposed to Pesticide in Martinique.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital Center of Martinique

About this trial

The CHLOR-DETOX study is a single-centre, double-blind, prospective, interventional, controlled, exploratory pilot study on subjects environmentally exposed to the organochlorine pesticide (kepone or chlordecone, CLD) in the French Caribbean (Martinique island). To our best knowledge, it is the first clinical trial in such subjects evaluating the potential effect of oral probiotic intake (Limosilactobacillus reuteri) on the reduction of CLD plasma levels (chlordeconemia) and fecal excretion, thus concurring to the reduction of CLD toxicity in study subjects.

Eligibility criteria

Qualifiers

Male or female, 18 years of age or older

Seen in clinical toxicology consultation at the CHU of Martinique during the study period

With an initial chlordeconemia > 1μg/L on a test less than 1 month old at the time of study inclusion

Affiliated to a social security scheme

Disqualifiers

History of cancer

Recent infections less than 6 months old

Known digestive diseases: chronic diarrhoea, ulcerative colitis, Crohn's disease, pancreatitis

Digestive procedures less than 6 months old.

Trial design

Treatments tested in this trial

  • Limosilactobacillus reuteri
  • Placebo

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University Hospital Center of Martinique

Lead sponsor

BioGaia AB

Collaborator

University Hospital, Limoges

Collaborator

Regional Health Agency, Martinique

Collaborator

Biological Resource Centre, Martinique

Collaborator

Reims University hospital

Collaborator