Prevention Clinical Trial
Official title:
A Monocentric, Comparative and Randomized Study on Pressure Ulcers Prevention With Mepilex® Border Sacrum Dressing in Scheduled Cardiovascular Surgery
The study is a randomised controlled trial of patients admitted for a scheduled cardiac
surgery at the Clermont-Ferrand hospital.
Patients meeting the study inclusion criteria will be allocated to either the control group
that will receive pressure ulcer prevention standard care or the intervention group that will
receive pressure ulcer prevention standard care plus have a Mepilex® Border dressing applied
to their sacrum.
The main objective of this research is to evaluate the impact of Mepilex Border® dressing
applied in addition to standard pressure ulcer prevention protocol, in a French hospital
setting, in at-risk patients in a cardiovascular surgery unit with full hospitalisation
including block operation and ICU.
Hypothesis: Patients treated with Mepilex® Border dressings will have a lower incidence rate
of sacral pressure ulcer development than patients receiving standard care.
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