Overview

Evaluation of the Depth and Duration of Anesthesia From Heated Lidocaine/Tetracaine (Synera®) Patches Compared With 5% Lidocaine (Lidoderm®) Patches Applied to Healthy Adult Volunteers

Status:
Completed

Trial end date:
2012-11-01

Target enrollment:

Participant gender:

Summary

This will be a randomized, single-blind, active-controlled, two-period crossover study in adult volunteers to compare the duration and depth of anesthesia between Synera® and Lidoderm® patches when applied for 30 minutes and 4 hours. The study will include a Screening Visit, two Treatment Periods, and a Follow-Up Phone Contact.

Phase:

Phase 1

Details

Lead Sponsor:

CRI Lifetree

Collaborator:

Nuvo Research Inc.

Treatments:

Anesthetics
Lidocaine
Tetracaine