The study will evaluate the safety and performance of the ESTYME® MATRIX Round and Anatomical Silicone Gel-Filled Breast Implants in the breast augmentation and reconstruction.
The study will evaluate the safety and performance of the ESTYME® MATRIX Round and Anatomical Silicone Gel-Filled Breast Implants in the breast augmentation and reconstruction at 3 months, 1 year and 2 years post-procedure
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Breast implant surgery in breast reconstruction or breast augmentation
Centre F.X. Michelet Chu Bordeaux
Bordeaux, France
Chu Pasteur
Nice, France
Clinique des Champs Elysées
Paris, France
Clinique BIZET
Paris, France
Local complications
Evaluation of the safety 3 months post-implantation. Procedure-related adverse events/complications at 3 months post implant. Main foreseen complications: infection, haematoma, wound healing complication, fluid accumulation, early capsular contracture, rupture, extrusion.
Time frame: 3 months
Satisfaction of the patient and the surgeon
Evaluation of the performance, 3 months post-implantation Performance endpoint will be assessed by implant procedure success at 3 months defined as follows: * satisfactory procedure duration for the surgeon * satisfactory size of the incision for the surgeon * implant correct placement (absence of visible deformation of the gel, absence of rotation for anatomical implants)
Time frame: 3 months
Local complications
Evaluation of the safety, 1 year and two years post-implantation. Safety endpoint: incidence of all Adverse Events (AE)/Serious Adverse Events (SAEs) @ 1 year and two years post procedure
Time frame: 1 year and 2 years
Satisfaction of the patient and the surgeon
Performance endpoints are as follows: * global surgeon satisfaction post-procedure assessed by the usability of the device during the procedure (current implant procedure): surgeon comfort level for the insertion/implantation of the prosthesis, * global patient and surgeon satisfaction @ 1 year and 2 years post-procedure
Time frame: 1 year and 2 years
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Institut du Sein
Paris, France
Hopital Tenon
Paris, France
Clinique Charcot
Sainte-Foy-lès-Lyon, France
Institut Gustave Roussy
Villejuif, France