Anesthetic Effect Duration Assessment

• Status: Completed
• Trial end date: 2012-05-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the duration of anesthetic effect produced , Lidocaine7% + Tetracaine 7% cream when applied with 2 different application times on the face and thigh.

• Phase: Phase 4
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Galderma; Galderma R&D
• Treatments: Anesthetics; Lidocaine; Tetracaine

Criteria

Inclusion Criteria:

• Healthy male of female subjects aged 18 or older with a normal not excessive hairy skin,

Exclusion Criteria:

• Female subjects who are pregnant or breast-feeding; or plan to become pregnant,

• Subjects who have a known allergy to one of the components of the test drug lidocaine, tetracaine or other local anesthetics,

• Subjects who are at risk in terms of precautions, warnings, and contra-indication with the study product.