N/A
21 Years
70 Years
21 Years
70 Years
Not Enrolling
Female
Breast Cancer
Female
Breast Cancer
Trial Information
Inclusion Criteria:
- Female age between 21-70 years.
- Subject has mammography or ultrasound findings
- Subject is scheduled for biopsy.
- Subject is scheduled for ultrasound breast scan.
- Subject understands the study procedure.
- Subject is willing to sign the inform consent and comply with the study
requirements.
Exclusion Criteria:
- Age < 21 years or > 70 years.
- Subject undergo previous breast surgery
- Known blood coagulation disorders.
- Known cardiac disorders.
- Breast infection / breast abscess / breast pains.
- Ipsilateral breast scar in same quadrant as current lesion
- Recent breast trauma.
- Pregnant or lactating woman
- Subject has bleeding disorder.
- Subject is suffering extreme general weakness.
- Subject objects to the study protocol.
- Physician objection.
- Known cognitive or psychiatric disorder
- Participation in any other clinical trial
Type of Study:
Interventional
Study Design:
Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
Outcome Measure:
Occurrences of adverse events
Outcome Time Frame:
immediately
Safety Issue:
Yes
Principal Investigator
Hanna Levy, PhD
Investigator Role:
Study Director
Investigator Affiliation:
Rambam Health Care Campus
Authority:
Israel: The Israel National Institute for Health Policy Research and Health Services Research
Study ID:
CBUS -RA-001
NCT ID:
NCT00355745
Start Date:
July 2006
Completion Date:
July 2009
Related Keywords:
- Breast Cancer
- Breast
- tumor
- ultrasound
- biopsy
- Breast mammographic or ultrasound findings
- Breast Neoplasms
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