Feasibility Study of Cavity Radiofrequency Ablation in ex Vivo Mastectomy Breast Tissue
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Details and patient eligibility
About
The purpose of this study is to build a device that will consistently ablate (destroy or remove) cavitary breast tissue after a formal breast cancer resection in order to mimic the tissue that is now irradiated after breast cancer lumpectomy. The device would be easier to handle, perform the ablation in less time and by so ablating this margin would avoid the need in many for reoperation to obtain negative margins and based on preliminary data avoid the need for radiation. This would be especially important in poor and rural patients and would lead to decreased costs of treatment in patients with favorable breast cancer.
Sex
Ages
Volunteers
Inclusion criteria
- Female
- Age greater than or equal to 18 years.
- Receiving bi-lateral mastectomy due to tumor in the breast, or by choice (prophylactic mastectomy). Only non-cancerous breast tissue will be included in the study.
- Ability to understand and the willingness to sign a written informed consent.
Exclusion criteria
- Those determined by the study investigator to have mental, physical, or medical conditions that would indicate that they should not participate.
- Because there is no patient contact with the device no medical contraindications are foreseen.
Trial design
Primary purpose
Allocation
Interventional model
Masking
0 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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