Soft Foam Dressings for Pressure Injury Prevention of Cardiac Surgery
Starting soon · Not applicable
Conditions studied: CAD - Coronary Artery Disease, CABG, Valve Disease, Heart, Aortic Diseases, Valve Heart Stenosis, Aortic Aneurysm, Mitral Disease, AORTIC VALVE DISEASES, Aortic Dissection
In brief
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.
Key facts
- Study ID
- NCT07379294
- Run by
- Shih,Wen-Chi
- People needed
- 80
- Starts
- 2026-05-31
- Expected to finish
- 2027-05-30
- Last updated by the study team
- 2026-05-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
- Intact skin without pre-existing pressure injury prior to surgery
You may not qualify if…
- 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
Full record on ClinicalTrials.gov
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