NCT01673542

Evaluating the Effectiveness of Dermal Analgesia Provided by the Application of Lidocaine and Prilocaine Cream 5% on the Puncture Site of Axillary Blocks

• Status: Completed
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 32 (actual)
• Sponsor: Poitiers University Hospital · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: —

Summary

Prospective Study, monocentric, controlled, randomized study. Evaluating the effectiveness of dermal analgesia provided by the application of Lidocaine and Prilocaine Cream 5% on the puncture site of axillary blocks.Our study includes 70 patients. Number of subjects required for a 50% difference with the standard deviation of the control group, a significance level of 5% for a 80% power, it takes 23 people per group. Objective power of 90% obtained with 35 patients per group. The expected benefit is the reduction of pain at the skin puncture during the realization of BAX. Improving professional practice and quality care

Conditions

• Surgery Scheduled

Interventions

Type	Name	Description
DRUG	Lidocaine-Prilocaine 5%
DRUG	DEXERYL

Timeline

• Start date: 2012-08-01
• Primary completion: 2013-05-01
• First posted: 2012-08-28
• Last updated: 2016-10-12

Locations

1 site across 1 country: France