ACTRN12615000667516
Completed
Phase 3
Randomised controlled trial of tissue adhesive, integrated securement products or external stabilisation devices versus standard care (bordered polyurethane) dressings to prevent central venous access device failure in intensive care patients with non-tunnelled, percutaneous central venous access devices: the CASCADE ICU trial
Associate Professor Marion Mitchell0 sites120 target enrollmentJune 26, 2015
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Central venous access device failure prior to completion of therapy
- Sponsor
- Associate Professor Marion Mitchell
- Enrollment
- 120
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Informed written consent
- •2\. Non\-tunnelled percutaneous CVAD to be inserted in ICU for clinical care for \>24 hours
Exclusion Criteria
- •1\. Peripherally inserted, tunnelled, dialysis, or pulmonary artery catheters;
- •2\. Current bloodstream infection;
- •3\. CVAD to be inserted through diseased, burned, scarred or hirsute skin;
- •4\. Allergy to any study product;
- •5\. Previous study enrolment in this admission
Outcomes
Primary Outcomes
Not specified
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