ACTRN12616001073493Completed未知
Randomised controlled trial of an integrated securement device (ISD) or tissue adhesive (TA) versus standard care (bordered polyurethane) dressings on intravascular catheter failure in paediatric patients
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Griffith University
- Enrollment
- 330
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Prevention
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- o limit to 18 Years (—)
- Sex
- All
Inclusion Criteria
- •1. Informed written consent
- •2. PVC in situ
- •3. PVC scheduled/expected use >24 hours
- •4. Patient aged 18 years or less.
- •5, Patient admitted to a Medical, Cardiac or Surgical ward
Exclusion Criteria
- •1. Known, current bloodstream infection (within 48 hours)
- •2. Non-English speakers without interpreter
- •3. PVCs inserted through diseased, burned or scarred skin
- •4. Other types of vascular access devices
- •5. Current skin tear/‘papery’ skin at high risk of tear
- •6. Known allergy to any study product
- •7. Previous enrolment in the current study
Investigators
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