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The Pharmacokinetics of 4% Lidocaine Gel When Applied Topically to the Breasts

Adverse Effects Clinical Trial

Official title:
The Pharmacokinetics of 4% Lidocaine Gel When Applied Topically to the Breasts

Clinical Trial Summary

The purpose of this study is to test the hypothesis that one-time application of 4% lidocaine gel (TOPICAINE) on the skin of the breasts and chest wall as recommended for pre-medication to reduce discomfort during screening mammography does not result in adverse effects, electrocardiogram (EKG) changes, or systemically toxic plasma concentration of lidocaine or its principal metabolite, monoethylglycinexylidide (MEGX).

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00925353
Study type Interventional
Source Mountain States Tumor and Medical Research Institute
Contact
Status Completed
Phase Phase 4
Start date January 2010
Completion date February 2010
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