Who is sponsoring NCT01688518?

NCT01688518 is sponsored by CRI Lifetree.

What drugs are being tested in NCT01688518?

Interventions: Heated Lidocaine/Tetracaine Patch, 5% Lidocaine Patch.

What is the status of NCT01688518?

NCT01688518 is currently COMPLETED.

Last reviewed 2013-01-02 · How we verify

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

NCT01688518 Phase 1 COMPLETED

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.

Details

Lead sponsor	CRI Lifetree
Phase	Phase 1
Status	COMPLETED
Enrolment	22
Start date	2012-09
Completion	2012-11

Conditions

Healthy

Interventions

Heated Lidocaine/Tetracaine Patch
5% Lidocaine Patch

Primary outcomes

Depth of Anesthesia measured in mm via insertion of 21-gauge needle into the skin. — Approximately 5 months

Countries

United States