Functional Microarray Augmentation of Skin Treatment With Lidocaine

Withdrawn before enrolling · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Pain Perception, Phlebotomy

In brief

The purpose of this study is to determine whether co-application of a functional microarray of needles (FMA) speeds the rate at which topical anesthesia is provided. A secondary goal is to determine whether the depth of anesthesia is enhanced.

Key facts

Study ID

NCT01145326

Run by

University of Oklahoma

People needed

0

Starts

2015-01-01

Expected to finish

2017-12-01

Last updated by the study team

2017-03-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• University of Oklahoma Schusterman Clinic — Tulsa, Oklahoma, United States

Full record on ClinicalTrials.gov

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