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
| Type | Name | Description |
|---|---|---|
| OTHER | Use of breast bra | Patients will use a breast from admission to hospital discharge |
| OTHER | Usual 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.