A randomized prospective simple-blind interventional study evaluating the efficacy of the
synthetic adhesive solution "Ifabond", in patients undergoing breast cancer surgery. The main
objective of this study is to determine if the application of Ifabond, in addition to the
conventional method of breast surgery, reduces the postoperative seroma formation. The
secondary objective is to assess quality of life immediately after surgery, and the need for
needle aspiration of the axilla, when using Ifabond.