Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Centre Hospitalier Universitaire de Besancon
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Female over 18 years of age
Diagnosis of invasive breast cancer (histological proof via breast biopsy)
Tumor size less than or equal to clinical T2 according to the current cTNM classification for breast cancer"
No clinical and/or radiological evidence of lymph node involvement
Affiliation to a French social security scheme or beneficiary of such a scheme
Approval in the multidisciplinary tumor board meeting for conservative treatment with partial mastectomy combined with sentinel lymph node biopsy
Signed informed consent indicating that the patient understands the purpose and procedures required by the study and agrees to participate in the study and comply with its requirements and restrictions
You may not be if
Severe and morbid obesity (BMI strictly greater than 35)
Emaciation (BMI strictly less than 18.5)
Contraindication to the medications used in the protocol
Contraindication to general anesthesia
Contraindication to the local anesthesia protocol
Tumor considered non-resectable under local anesthesia according to the surgeon's assessment
Bifocal tumor
Associated oncoplastic procedure
Contralateral surgical procedure (implantable port placement, mastopexy, partial or total mastectomy)
Withdrawal of consent prior to surgery
Legal incapacity or limited legal capacity
Non-fluency in the French language or poor understanding as anticipated by the investigator
Subject without health insurance
Pregnant woman
Subject currently in the exclusion period of another study or listed in the national volunteer registry
Clareo Health | Evaluation of the Feasibility of a Study Comparing Local Anesthesia and General Anesthesia in Conservative Surgery for Breast Cancer
