Malignant neoplasm of breast of unspecified site
Conditions
Interventions
This is a prospective randomized trial with breast cancer patients undergoing oncology surgery following breast reconstruction. A total of 100 patients were randomized to simulation or not at preopera
Sponsors
Universidade Positivo
Hospital Nossa Senhora das Graças
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Breast cancer patients with carcinoma in situ or invasive carcinomas undergoing oncology surgery following breast reconstruction or oncoplastic surgery
Exclusion criteria
Exclusion criteria: Patients who refused and could not complete six month follow-up; who underwent prophylactic mastectomy or preoperative radiotherapy; those who had local recurrence or metastasis at the time of analysis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: It is expected to find a relationship between the application of the 3D software in the preoperative consultation and the satisfaction of the patient undergoing breast reconstruction through the BREAST-Q questionnaire ;Result found 1: When Breast-Q score were compared between groups who received 3D simulation or not, the intervention group who had 3D simulation were more satisfied with information than the control group (p =0.021) | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: Evaluate whether the software contributes to the patient understand better about your surgery;Result found 2: The 3D simulation really helps the patients understanding the process of surgery in the preoperative set(86,6% oncoplastic group and 75% breast reconstruction group) | — |
Countries
Brazil
Contacts
Public ContactFlávia kuroda
Hospital Nossa Senhora das Graças
Outcome results
None listed