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Kinetic Time Courses of Bisphenol-S in Volunteers

NCT03340168 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2018-05-09

No results posted yet for this study

Summary

The time course of bisphenol S in plasma and urine will be monitored in female adults exposed to a single oral and dermal dose of bisphenol-S. Six female will be recruited. Blood and urine will be collected at specified times post-treatment. Bisphenol concentrations will be measured in those samples.

Conditions

  • PHARMACOKINETICS

Interventions

OTHER

Bisphenol-S

Oral and dermal exposure in volunteers

Sponsors & Collaborators

  • Université de Montréal

    lead OTHER

Principal Investigators

  • Michèle Bouchard, PhD · Université de Montréal

Study Design

Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
25 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-03-05
Primary Completion
2020-12-31
Completion
2020-12-31

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03340168 on ClinicalTrials.gov