Anesthetic Effect Duration Assessment

Completed · Phase 4

Conditions studied: Healthy Volunteers

In brief

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.

Key facts

Study ID

NCT01545765

Run by

Galderma R&D

People needed

30

Starts

2012-05-01

Expected to finish

2012-05-01

Last updated by the study team

2021-09-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

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

You may not qualify if…

• 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.

Where it is running

• Galderma Investigational center — Rochelle Park, New Jersey, United States

Full record on ClinicalTrials.gov

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