Wound Healing Clinical Trial
Official title:
Randomized Controlled Trial of the Effectiveness of Bra Application in Women as a Device for Prevention of Surgical Wound Dehiscence in the Post-operative Cardiac Surgery
The aim of the study was to assess the efficacy of bra application as a prevention of dehiscence in women with median sternotomy.
Background: it is known that the size and support of the breasts are a specific problem in
post-operative women of cardiac surgery by means of medium sternotomy. There is little
evidence of the therapeutic action of the bra as a measure to prevent dehiscence of the
surgical wound.
Aim: To assess the efficacy of bra application as a prevention of dehiscence in women with
median sternotomy.
Methods: Randomised clinical trial; post-test control group in women undergoing cardiac
surgery by mean sternotomy. Groups: application of post-surgical or non-surgical breast bra.
Endpoint: incidence of dehiscence. Other variables: sociodemographic, signs of infection,
pain, related to assessment of the wound on admission. Assessment of the surgical wound
daily, at discharge, at month, 3 months and 6 months post discharge.
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