breast cancer carcinoma of the breast
Conditions
Interventions
None listed
Sponsors
Leids Universitair Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Women who have undergone breast conserving surgery for early breast cancer more than one year ago. Written informed consent obtained.
Exclusion criteria
Exclusion criteria: Unable to provide written informed consent. Younger than 18 years. Benign breast disease. Women who have had a mastectomy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective will be to create a reliable demonstrator (software) by integrating models of surgical techniques and treatment schemes, clinical patient data, multimodal imaging and individualised models of patient anatomy. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objective will be to assess the health related quality of life in the women who are participating in this study. The information obtained from this study will be used in the creation of a demonstrator (personalised digital representation of a patient) by integrating models of surgical techniques and treatment schemes, clinical patient data, multimodal imaging and individualised models of patient anatomy. The aim is to create a demonstrator that will be used as an aid to objective surgical planning, via simulation of the cosmetic effects of breast conserving surgery, as a decision support tool to communicate the available options to the patient and to enable standardised evaluation of the procedure. | — |
Countries
Netherlands
Outcome results
None listed