Soft Foam Dressings for Pressure Injury Prevention of Cardiac Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorShih,Wen-Chi

About this trial

The purpose of this study is to evaluate whether the application of soft foam dressings can reduce the occurrence of surgery-related pressure injuries among patients undergoing cardiac surgery. Specifically, this research aims to investigate differences in pressure injury outcomes before and after the intervention, and to assess the preventive effectiveness of soft foam dressings as an adjunctive skin-protection strategy.

Eligibility criteria

Qualifiers

Adults aged 18 years or older

Scheduled to undergo cardiac surgery under general anesthesia

Use of cardiopulmonary bypass (CPB) during surgery

Expected surgical duration greater than 4 hours

Disqualifiers

Surgical position other than supine

Long-term bedridden status prior to hospital admission

Altered consciousness or inability to cooperate

History of stroke with residual limb weakness

Trial design

Treatments tested in this trial

  • CONVAFoam Hydrofiber Dressing
  • Standard Pressure Injury Prevention Care

Treatment groups

80 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Shih,Wen-Chi

Lead sponsor

Fu Jen Catholic University Hospital

Sponsor institution