Clinical Trials Directory

Trials / Completed

CompletedNCT04290260

Use of the Bra as Prevention of Sternal Wound Dehiscence in Cardiac Surgery

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Germans Trias i Pujol Hospital · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the study was to assess the efficacy of bra application as a prevention of dehiscence in women with median sternotomy.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
OTHERUse of breast braPatients will use a breast from admission to hospital discharge
OTHERUsual care (not use of bra)

Timeline

Start date
2015-01-01
Primary completion
2016-11-01
Completion
2016-11-01
First posted
2020-02-28
Last updated
2020-02-28

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04290260. Inclusion in this directory is not an endorsement.