drugset / Trial / NCT01673542

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

NCT01673542

Phase 2 Completed 32 enrolled Poitiers University Hospital

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

Timeline

Start
2012-08
Primary completion
2013-05
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Lidocaine-Prilocaine Unknown 5 % Topical

Indications

No indication recorded.