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Clinical Trials/ACTRN12616001174471
ACTRN12616001174471
Completed
未知

Efficacy of nasogastric and endotracheal tube securement devices, preventative dressings and topical skin applications for reducing device-related pressure injuries in intensive care patients; a pilot study

Queensland University of Technology0 sites100 target enrollmentAugust 26, 2016

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Queensland University of Technology
Enrollment
100
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 26, 2016
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All ICU patients \= or \>18 years who have a NGT and/or ETT in situ
  • Patients who are expected to remain in ICU \> 24 hours
  • NGT or ETT inserted a maximum of 12 hours prior to ICU admission
  • Patients readmitted to ICU with no oral or nasal skin injury present
  • NGT arm only \- must have wide bore NGT and an ETT in situ.

Exclusion Criteria

  • Burn patients with an ETT wired in place (ETT arm only)
  • Patients with NGT sutured in place or nasal bridle (NGT arm only)
  • Patients with facial trauma
  • Traumatic brain injured patients requiring intracranial pressure monitoring and/or ventricular drainage of cerebrospinal fluid
  • Cervical spine injured patients who have a hard collar in situ
  • Hirsute patients with beards where patient permission to shave is not possible
  • Patients who are receiving non\-invasive ventilation
  • Patients with a device (NGT or ETT) predicted to be in situ \< 48 hours.
  • Patients with a community or hospital\-acquired NGT or ETT PI diagnosed within 24 hours of admission to the ICU.
  • Patients on whom treatment is withdrawn or who are being palliated.

Outcomes

Primary Outcomes

Not specified

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