The Effect of Silicone Foam Dressing and Repositioning on the Prevention of Endotracheal Tube-related Pressure Injuries

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHacettepe University

About this trial

The endotracheal tube is one of the medical devices most associated with pressure injuries related to medical devices. This study aims to evaluate the effectiveness of applying a silicone foam dressing over the endotracheal tube and repositioning the endotracheal tube in preventing endotracheal tube-related pressure injuries in patients receiving mechanical ventilation support.

Eligibility criteria

Qualifiers

Aged 18 years or older

Patients admitted to the General Intensive Care Unit and receiving mechanical ventilation support

Absence of pressure injuries, other lesions, or anomalies on the inner and outer surfaces of the lips and at the oral commissures prior to intubation

Absence of congenital anomalies that could interfere with the assessment of pressure injuries on the inner and outer surfaces of the lips and at the oral commissures

Disqualifiers

Receiving mechanical ventilation support initiated prior to admission to the intensive care unit

Undergoing nasotracheal intubation

History of any intraoral surgical procedure

Presence of a contraindication to repositioning of the endotracheal tube

Trial design

Treatments tested in this trial

  • Use of silicone foam dressing and repositioning every 8 hours
  • Repositioning every 8 hours

Treatment groups

75 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators