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
Locations
Sponsors and collaborators
Shih,Wen-Chi
Lead sponsor
Fu Jen Catholic University Hospital
Sponsor institution