A clinical evaluation of two central venous catheter stabilization systems

niversity Hospitals Birmingham NHS Foundation Trust0 个研究点目标入组 186 人开始时间: 2015年7月9日最近更新: 2019年5月13日

试验速览

•1. =18 years of age
•2. Admitted, or to be admitted, to a critical care unit
•3. Require a single, short-term, non-cuffed, non-tunnelled CVC (up to and including 12F in size) as part of their clinical care
•4. Willing and able to provide written informed consent (or if their condition do not allow this their legally authorized representative willing and able to give the consent on their behalf)

•1. Confused (patients who have a positive CAMICU score or if confusion expected after sedation stopped)
•2. Excessively perspiring (skin becomes moist within 2 minutes of drying)
•3. Non adherent skin burn, trauma or other condition affecting the skin integrity in close proximity to the potential insertion site, so that the device/ suture is applied to the skin without any of these conditions
•4. Underlying uncorrected bleeding diathesis
•5. Known allergy to adhesives or device components
•6. To have more than one catheter inserted at the same location
•7. Pregnant or breastfeeding women
•8. Past participants in this study

发起方

niversity Hospitals Birmingham NHS Foundation Trust