Status:
UNKNOWN
Using Test of SCM for Detection Breast Cancer
Lead Sponsor:
Ziv Hospital
Conditions:
Malignant Breast Cancer, Benign Breast Lesions
Eligibility:
FEMALE
18-50 years
Brief Summary
In our previous research, we have shown that women that have breast cancer have a population of lymphocytes that recognizes specific antigen and there cytoplasmic matrix goes through physical change a...
Eligibility Criteria
Inclusion
- Women carrying benign breast lesions will be further divided and analyzed according to the Fitzgibbon's risk categories for invasive cancer risk (4). The Fitzgibbon's categories are:
- No increased risk group including adenosis (other than sclerotic), duct ectasia fibroadenoma without complex features,
- slightly increased risk group (1.5-20 times) which includes fibroadenoma with complex features, moderate or florid hyperplasia without atypia, sclerosing adenosis,
- moderately increased risk group (4.0-5.0 times) includes atypical ductal and lobular hyperplasia and
- markedly increased risk group (8.0-10.0 times) which includes ductal and lobular carcinomas In Situ Following the blood collection, detailed relevant clinical information of the patient will be registered in a case record form.
- The data will include: age, country of birth, last menstrual period, lactation, number of children, age at first full-term pregnancy, age at onset of menopause, family history, medication, mammography findings, FNA results, tumor size, histological findings, biopsies, disease staging, and other relevant clinical information.
Exclusion
- pregnancy,
- experiencing menstruation, or
- under hormonal or drug treatment.
Key Trial Info
Start Date :
December 1 2006
Trial Type :
OBSERVATIONAL
End Date :
December 1 2010
Estimated Enrollment :
180 Patients enrolled
Trial Details
Trial ID
NCT00407706
Start Date
December 1 2006
End Date
December 1 2010
Last Update
December 5 2006
Active Locations (1)
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1
Surgery Department
Safed, Israel, 13110