Clinical Trials Directory

Trials / Unknown

UnknownNCT04788810

Toxicokinetic Study of Dichlorobisphenol A After an Oral or Dermal Single Dose in Healthy Volunteer.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
12 (estimated)
Sponsor
Poitiers University Hospital · Academic / Other
Sex
Female
Age
18 Years – 51 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to determine toxicokinetic parameters of deuterated d12-Cl2BPA after the administration of a single low dose (50 µg/kg) to healthy volunteers via oral or dermal routes.

Detailed description

Dichlorobisphenol A (Cl2BPA)is formed by the reaction of chlorine with bisphenol A present in water during water disinfection process. As a consequence, Cl2BPA is present in various aqueous media including tap water. Cl2BPA has also been found in human, in blood, urine, breast milk and adipose tissue suggesting chronic exposure to this compound. Cl2BPA is an endocrine disruptor that binds to estrogenic and PPAR-γ receptors. Epidemiological studies have shown that exposure to DCBPA has been related to the occurrence of diabetes, obesity and myocardial infarction. Currently, no toxicokinetic data are available to estimate the disposition (ADME) of Cl2BPA after oral and dermal exposure in human while these data are needed for proper risk assessment of this compound. The objective of this study is to determine toxicokinetic parameters of deuterated d12-Cl2BPA after the administration of a single low dose (50 µg/kg) to healthy volunteers via oral or dermal routes.

Conditions

Interventions

TypeNameDescription
OTHERAdministration of d12-Cl2BPAAdministration of d12-Cl2BPA

Timeline

Start date
2021-03-01
Primary completion
2022-03-01
Completion
2022-09-01
First posted
2021-03-09
Last updated
2021-04-05

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04788810. Inclusion in this directory is not an endorsement.