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
Completed · Phase 1
Conditions studied: Healthy
In brief
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.
Key facts
- Study ID
- NCT01688518
- Run by
- CRI Lifetree
- People needed
- 22
- Starts
- 2012-09-01
- Expected to finish
- 2012-11-01
- Last updated by the study team
- 2013-01-04
Who can join
Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.
Where it is running
- Lifetree Clinical Research — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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