Evaluate the Depth and Duration of Anesthesia

Completed · Phase 4 · Has a placebo group

Conditions studied: Pain

In brief

The purpose of the study is to determine the depth (mm) of anesthesia provided by the Synera topical patch (using sensory depth and pain depth evaluations), and to determine the duration (minutes) of anesthesia provided by the Synera topical patch (using dermal sensory testing and thermal sensory testing evaluations), compared with a matching heated placebo patch.

Key facts

Study ID

NCT00891163

Run by

ZARS Pharma Inc.

People needed

25

Starts

2006-12-01

Expected to finish

2007-04-01

Last updated by the study team

2009-05-01

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Had no known significant diseases
• Normal 12-lead electrocardiogram
• Willing to refrain from using any local topical preparations

You may not qualify if…

• Taken over-the-counter (OTC) or prescription analgesics in any form within 24 hours
• Known allergy or sensitivity to any component of the Synera patch, including lidocaine, sympathomimetic amines, other local anesthetics of the amide type, epinephrine, or other patch components
• Had an active dermatological disease of any origin that may have interfered with their ability to participate

Where it is running

• UCSD Medical Center, Thornton Hospital — San Diego, California, United States

Full record on ClinicalTrials.gov

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