Clinical Evaluation of OSNA Breast Cancer System to Extensive Frozen Section Histopathology
Launched by SYSMEX AMERICA, INC. · Jun 6, 2011
Trial Information
Current as of October 12, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Male or female;
- • 18 years of age or older;
- • Diagnosed pre-surgically with T1 or T2 breast cancer without clinical evidence of axillary lymph node involvement and scheduled for surgery including sentinel lymph node dissection;
- • Subjects (or the subjects' legal representatives) who have read, understood to the best of their ability and signed the informed consent form.
- Exclusion Criteria:
- • Subjects diagnosed pre-surgically with large or locally advanced (T3 \& T4) breast cancer;
- • Pregnant subjects, confirmed by interview with either subject or treating physician;
- • Subjects diagnosed with inflammatory breast cancer;
- • Subjects diagnosed with ductal carcinoma in situ (DCIS) when breast conservation is to be done;
- • Subjects with clinically suspicious, palpable axillary lymph nodes;
- • Subjects previously treated for or previously diagnosed with another type of invasive cancer. Subjects with skin cancer (basal cell and squamous cell carcinoma) may be included, except for subjects diagnosed with melanoma; Subjects with non-invasive carcinoma of the Cervix may also be included in this study.
- • Subjects who have received pre-operative systemic therapy;
- • Subjects who are incapable of providing written informed consent;
- • Subjects who have been judged to be an inappropriate candidate by any medical care provider (e.g., surgeon, oncologist or pathologist).
- • Subjects participating in other clinical studies where the SLN evaluation will be negatively impacted by this study.
About Sysmex America, Inc.
Sysmex America, Inc. is a leading global provider of advanced diagnostic and healthcare solutions, specializing in laboratory instrumentation and information systems. With a strong commitment to innovation and excellence, Sysmex America focuses on enhancing patient care through the development of cutting-edge technologies in hematology, urinalysis, and coagulation diagnostics. The company actively engages in clinical trials to evaluate the efficacy and safety of its products, ensuring they meet the highest standards of quality and reliability. Sysmex America is dedicated to collaborating with healthcare professionals and institutions to improve diagnostic accuracy and streamline laboratory workflows, ultimately contributing to better patient outcomes.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Milan, Italy
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials