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Clinical Trials/ACTRN12614001329651
ACTRN12614001329651
Completed
未知

Randomised controlled trial of tissue adhesive, combined securement and dressing product or external stabilisation devices versus standard care (bordered polyurethane) dressings to prevent central venous access device failure in paediatric intensive care patients with percutaneous central venous access devices: the CASCADE Junior PICU trial

Griffith University0 sites80 target enrollmentDecember 17, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Central venous access device failure and complication prior to completion of therapy
Sponsor
Griffith University
Enrollment
80
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 17, 2014
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • \*Patient requires the insertion of a percutaneous CVAD for \>24 hours;
  • \*Will remain in admitted to the RCH/LCCH for \>24 hours;
  • \* Less than 16 years of age; and
  • \*Parent or legal guardian, and child if developmentally appropriate, gives informed consent.

Exclusion Criteria

  • \*Tunnelled, peripherally inserted, dialysis, or implanted CVADs or pulmonary artery catheters;
  • \*Current bloodstream infection;
  • \*CVAD to be inserted through diseased, burned or scarred skin;
  • \*Allergy to study product; and
  • \*Previous study enrolment in this admission to hospital

Outcomes

Primary Outcomes

Not specified

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