Protocol
06-076
Full Title
Inamed Corporation Style 410 Silicone-Filled Breast Implants Continued Assess Reconstruction Revision Expansion (CARE) Clinical Study
Purpose
The purpose of this study is to evaluate the safety and effectiveness of the Inamed Corporation Style 410 silicone-filled breast implant in women who are candidates for breast reconstruction or revision. Researchers will collect 10 years of data from women who receive these implants as part of this study. These data will include answers to questionnaires about activities, lifestyle, and (for reconstruction patients) quality of life. Photographs will also be taken of the breast/chest area one year after surgery by the surgeon or his/her staff. These photographs will remain confidential.
Investigator
Eligibility
To be eligible for this study, patients must meet several criteria, including but not limited to the following:
- Participants will include women who are candidates for breast reconstruction following mastectomy, or removal or replacement of prior breast implants.
- The implantation must be performed by a surgeon at Memorial Sloan-Kettering Cancer Center.
- Participants must agree to return for all follow-up visits.
- Participants must be age 18 or older.
For more information and to see if you are eligible for this study, please contact Dr. Peter Cordeiro at 212-639-2521.
Disease(s)
Breast Cancer
Survivorship
Locations
Related Diseases
