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Clinical Trials/NCT01842373
NCT01842373
Withdrawn
Not Applicable

A Double-Blind, Randomized, Split-Face Comparison Trial on Topical Anesthetic Agents Prior to Fractional Skin Resurfacing

Milton S. Hershey Medical Center1 site in 1 countryJuly 2013
ConditionsPain
InterventionsBLTLMX4
DrugsLMX4BLT

Overview

Phase
Not Applicable
Intervention
BLT
Conditions
Pain
Sponsor
Milton S. Hershey Medical Center
Locations
1
Primary Endpoint
Patient Assessment of Pain
Status
Withdrawn
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this research study is to test which topical anesthesia: LMX4 (Lidocaine 4%) or BLT (Benzocaine 20%, Lidocaine 6%, and Tetracaine 4%) is more effective in reducing discomfort during treatment with the Fraxel DUAL 1550/1927 (Solta Medical, Hayward, CA). No studies have been done on the effectiveness of LMX4 versus BLT using the Fraxel DUAL, although individually LMX4, BLT, and the Fraxel DUAL have been studied extensively.

The hypothesis is that there will be no clinical difference between the two topical anesthetics.

Detailed Description

Lasers can be effectively utilized for facial rejuvenation, reduction of photoinduced rhytides, and dyschromia. Topical anesthetics are used to minimize the discomfort associated with laser induced thermal pain. There are currently several formulations of topical anesthesia. However, studies comparing the products are limited especially for the new formulations that claim increased efficacy and faster onset. LMX4 (Ferndale Laboratories, Ferndale, Michigan) is over the counter topical anesthesia. It is 4% lidocaine that has been formulated into multilamellar vesicles containing several lipid bilayers. This unique liposomal-based delivery system has been reported to deliver a greater concentration of drug. This results in a longer duration of activity and faster onset of action without requiring occlusion.4 Liposomes assist with drug penetration because the skin is lipid bilayer that can encapsulate the drug. BLT is a compounded topical anesthetic containing 20% benzocaine, 6% lidocaine, and 4% tetracaine. It is commonly prescribed as topical anesthesia. All BLT products will be compounded at the University Physicians Center Pharmacy to ensure safety and uniformity. Anecdotally, some physicians claim it is the topical anesthesia of choice prior to laser surgery. The objective of the study is to evaluate the clinical efficacy of topical anesthetic compounds prior to fractional skin resurfacing.

Registry
clinicaltrials.gov
Start Date
July 2013
End Date
December 2013
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Charlene Lam

Resident Physician

Milton S. Hershey Medical Center

Eligibility Criteria

Inclusion Criteria

  • At least 28 subjects will be included in this study.
  • Subjects capable of giving informed consent.
  • Patients 18 years of age and older will be included in this study.
  • Any patient seeking Fraxel DUAL1550/1927 (Solta Medical) treatment on the face for rhytids, photoaging, hyperpigmentation, and acne scarring at the Hershey Medical Center dermatology clinics will be asked to participate.

Exclusion Criteria

  • Allergy to lidocaine or tetracaine
  • Women who are pregnant or breast-feeding
  • Patients with cardiac or respiratory disease, seizure disorders, or neuropathy
  • Patients currently taking anxiolytics and opiates

Arms & Interventions

LMX4

3 g of LMX4 will be applied to one half of the face for 60 minutes

Intervention: BLT

BLT

3 g of BLT will be applied to half of face for 60 minutes

Intervention: LMX4

Outcomes

Primary Outcomes

Patient Assessment of Pain

Time Frame: Immediately after laser treatment

A pain assessment will be performed on both halves of the face by utilizing a standard 10 cm visual analog pain scale (VAS).

Study Sites (1)

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