Clinical Trials Directory

Trials / Completed

CompletedNCT00572884

Metabolism of the Insecticide Permethrin

CCRC:Identification and Development of Biological Markers of Human Exposure to the Insecticide Permethrin

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
6 (actual)
Sponsor
University of California, Davis · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

Military personnel are exposed to the insecticide permethrin when using the DOD Insect Repellent System. A urinary metabolite of permethrin that is in high abundance and is relatively stable may be an ideal biomarker of exposure to this pesticide. Monitoring such a biomarker can prevent over-exposure. The objectives are to identify the most abundant human urinary metabolite following dermal exposure; to utilize this information to develop rapid laboratory-based and field portable methods to monitor the degree of an individual's exposure to permethrin.

Detailed description

Permethrin is applied to the forearm of the subject and remains for 8 hours. The exposed area is then washed with soap and water several times. 24 hour urine samples are collected at daily intervals for 192 hours. Blood and saliva samples are taken at pre-dose, 1, 3, 6, 9 12, 24, 48, 72, 96, 120, 144, 168 and 192 hours. Subjects must return to the clinic daily to drop off urine collections and have blood and saliva samples taken.

Conditions

Interventions

TypeNameDescription
OTHERpermethrin insecticide25 mg neat carbon-14 labelled permethrin applied dermally in isopropyl alcohol, once for 8 hours containing 1 microcurie of carbon-14

Timeline

Start date
2006-02-01
Completion
2007-11-01
First posted
2007-12-13
Last updated
2007-12-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00572884. Inclusion in this directory is not an endorsement.