EUCTR2005-005960-95-GB进行中（未招募）1 期
Prospective, randomised clinical trial to compare the efficacy of 0.5% (w/v) chlorhexidine gluconate in 70% (v/v) isopropyl alcohol with 2% (w/v) chlorhexidine gluconate in 70% (v/v) isopropyl alcohol (Chloraprep) for the pre-operative disinfection of skin prior to coronary artery bypass grafting and post operative wound care. - Evaluation of Chloraprep for skin disinfection
Enturia, Inc.0 个研究点目标入组 676 人开始时间: 2006年2月17日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 676
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •Must be at least 18 years of age.
- •Require coronary artery bypass grafting
- •Donor vein retrieval from the leg (saphenous veins)
- •Willing and able to provide informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Psychiatric history or mental handicap
- •Breast feeding females or pregnancy
- •Patients with a known history of chlorhexidine allergy
- •Patients with dermatoses, inflammation or injuries to the donor site.
研究者
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