Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Case Comprehensive Cancer Center
Primary Endpoint(s)
1. Define the optimal timing of reconstruction in patients at a higher risk for developing breast reconstruction surgical complications through a randomized prospective cohort
2. Compare immediate and delayed reconstruction outcome metrics through retrospective review
Secondary Endpoint(s)
1. Evaluate Quality of life of patients at a higher risk for developing breast reconstruction surgical complications undergoing immediate versus delayed reconstruction.
2. Compare complications and reoperations between immediate versus delayed reconstruction.
3. Compare the hospital costs between immediate versus delayed reconstruction
4. Evaluate the effectiveness of risk reduction strategies
Age
19–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Subjects must have histologically or cytologically confirmed breast cancer or indication for prophylactic mastectomy.
Subjects must be breast reconstruction candidates using implant based breast reconstruction.
Subjects must have a pre-operative risk \>20% complication prediction from the Breast Reconstruction Risk Assessment (BRA) Score for implant-based breast reconstruction candidates
Subjects must have the ability to understand and the willingness to sign a written informed consent document.
