NCT00562211

Efficacy of a New Topical Anesthetic

A Single-blind, Randomized, Controlled Trial to Assess the Efficacy of a New Topical Anesthetic in Reducing Pain Associated With Venipuncture in Children.

• Status: Completed
• Phase: Phase 1 / Phase 2
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: Rambam Health Care Campus · Academic / Other
• Sex: All
• Age: 12 Years – 16 Years
• Healthy volunteers: Accepted

Summary

A new topical anesthetic which contains 5% lidocaine and a disinfection ingredient has been developed and is tested in this study (LidoDyn). The study examines the efficacy of LidoDyn by comparing it with an already proven anesthetic agent (EMLA crème).

Conditions

• Pain

Interventions

Type	Name	Description
DRUG	LidoDyn	Application of 2 gram of LidoDyn to the skin surface the patient's antecubital fossa 60 min prior to venipuncture
DRUG	EMLA creme	Application of 2 gram of EMLA creme to the skin surface the patient's antecubital fossa 60 min prior to venipuncture

Timeline

• Start date: 2007-11-01
• Primary completion: 2008-04-01
• Completion: 2008-04-01
• First posted: 2007-11-21
• Last updated: 2014-05-06

Locations

1 site across 1 country: Israel