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A Comparison of Recall Rates Between Conventional 2d Mammography and 2d Plus 3d (Tomosynthesis) Mammography in a Screening Population
Conditions
Breast Cancer
Conditions: Keywords
breast cancer screening, tomosynthesis, FFDM
Study Type
Observational
Study Phase
N/A
Study Design
Observational Model: Cohort, Time Perspective: Retrospective
Overall Status
Recruiting
Summary
The primary aim of this study is to measure, document and compare recall rates of two-dimensional plus three dimensional (2D plus 3D) (Tomosynthesis) mammography to that of 2D mammography in a screening population. This study will compare recall rates for both non-cancer and cancer cases.
Criteria for eligibility
Healthy Volunteers: Accepts Healthy Volunteers
Maximum Age: N/A
Minimum Age: 30 Years
Gender: Female
Criteria: Inclusion Criteria:
- Subject is female of any race and ethnicity
- The subject is asymptomatic and presents for routine screening mammography and chooses to have a combination 2D + 3D mammogram as her standard of care.
Exclusion Criteria:
- Patient chooses standard 2D mammography over a combination 2D + 3D mammogram
- Subject is female of any race and ethnicity
- The subject is asymptomatic and presents for routine screening mammography and chooses to have a combination 2D + 3D mammogram as her standard of care.
Exclusion Criteria:
- Patient chooses standard 2D mammography over a combination 2D + 3D mammogram
Location
TOPS
Houston, Texas, United States
Status: Recruiting
Contact: Andra Tidwell, RT(R)(M) - 281-580-6171 - atidwell@uspi.com
Start Date
January 2012
Sponsors
Rose Imaging Specialists, P.A.
Source
Rose Imaging Specialists, P.A.
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page