Prospective, double-blind, randomized controlled single-centre trial: suppression of surgeons? skin flora during surgical procedures using a new antimicrobial surgical glove

Ansell Healthcare (Belgium)0 个研究点目标入组 52 人开始时间: 2012年5月8日最近更新: 2019年2月11日

适应症

试验速览

•1. All surgeons agreeing to participate after appropriate orientation and instruction
•2. Surgeons with visibly healthy skin, without cuts or abrasions, and individuals who had not used medicated soap or medicated hand creams one week prior to the test run
•1. All patients undergoing carotid endarterectomy, aortic reconstruction for aneurysms or occlusive disease, or open surgical bypass for peripheral arterial occlusive disease, are eligible to be included into the study if no existing infection at any site is present.
•2. Patients must not have a re-operation during the subsequent 30 days before the study

•1. Individuals without visibly healthy skin, with cuts or abrasions, and individuals who had used medicated soap or medicated hand creams one week prior to the test run
•2. The use of alcohol-based hand rubs containing no additional compounds with a sustained antimicrobial efficacy 24 hours before testing
•1. All patients for which all other procedures are performed than carotid endarterectomy, aortic reconstruction for aneurysms or occlusive disease, or open surgical bypass for peripheral arterial occlusive disease
•2. All patients with an existing infection at any site and patients having a re-operation during the subsequent 30 days

发起方

Ansell Healthcare (Belgium)