Breast Cancer Clinical Trial
— SiennaOfficial title:
Sentinel Lymph Node Biopsy Using a Magnetic Tracer Versus Standard Radio-isotope Technique in Early Breast Cancer
The aim of this study is to evaluate a new method for the localization of breast cancer sentinel lymph node using Sienna+® and Sentimag® detection in comparison to our standard techniques with radio-isotopes.
Status | Not yet recruiting |
Enrollment | 52 |
Est. completion date | December 31, 2018 |
Est. primary completion date | December 31, 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Women diagnosed with early-stage breast cancer (including ductal carcinoma in-situ) who are clinically or radiologically node-negative and consenting for sentinel lymph node biopsy - Patients undergoing SNOLL (Sentinel node and occult lesion localization) with the use of radio-isotope in our Breast Centre Exclusion Criteria: - Patients with clinically T3 or T4 breast cancer and any contraindication to sentinel lymph node biopsy - Patients with pacemaker or other implantable device in the chest wall |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Yolanda Chan |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of successful procedures for sentinel lymph node identification (identification rate per patient) by the magnetic method compared with the standard method | Two years |
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