Clinical Evaluation of OSNA Breast Cancer System in Breast Cancer Patients Receiving Neoadjuvant Therapy
Stopped early
Conditions studied: Breast Neoplasms, Breast Diseases
In brief
The study will determine the sensitivity, specificity, negative predictive value and positive predictive value of the OSNA Breast Cancer System for patients receiving Sentinel Lymph Node biopsies after receiving neoadjuvant hormonal/chemotherapy as compared to permanent section Hematoxylin and Eosin (H\&E) and Immuno-histochemistry (IHC) staining.
Key facts
- Study ID
- NCT01140776
- Run by
- Sysmex America, Inc.
- People needed
- 100
- Starts
- 2010-11-01
- Expected to finish
- 2012-07-01
- Last updated by the study team
- 2011-06-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female
- 18 years of age or older
- Diagnosed pre-surgically with T1-T3 or T4 non-inflammatory breast cancer, clinically node positive or node negative upon clinical examination
- Scheduled for SLN biopsy after receiving neoadjuvant hormonal or chemotherapy
- Subjects (or the subjects' legal representatives) who have read, understood (to the best of their ability) and signed the informed consent form.
You may not qualify if…
- Pregnant subjects, confirmed by interview with either subject or treating physician
- Subjects previously diagnosed with other invasive cancer. Subjects with skin cancer (basal cell and squamous cell carcinoma) may be included, except for subjects diagnosed with melanoma
- Participation in other neoadjuvant protocols specifically requiring SLN biopsy prior to administration of neoadjuvant chemotherapy or hormonal therapy
- Subjects who have been judged to be an inappropriate candidate by any medical care provider (e.g., surgeon, oncologist or pathologist).
Where it is running
- Arizona Cancer Center — Tucson, Arizona, United States
- University of Texas MD Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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