The purpose of this study is to evaluate the clinical feasibility and safety of the ICESENSE3TM cryotherapy system for the ablation of small malignant invasive breast tumors.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
4
Ice-Sense Cryoprobe
Oncogynecological Center, Department of Obstetrics and Gynecology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague Prague, Czech Republic
Prague, Czechia
The rate of complete tumor ablation in patients treated with cryoablation, with complete tumor ablation defined as no remaining invasive or in-situ carcinoma present upon pathological examination of the surgical resection specimen
Time frame: One month
Adverse events
To describe the adverse events associated with cryoablation in these patients.
Time frame: One month
Pain assessment
To prospectively gather pain assessment data before and after cryoablation and after surgical resection in these patients
Time frame: One month
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