Comparison of Conspicuity of Masses and Architectural Distortions Between Wide- and Narrow-angle Digital Breast Tomosynthesis Systems

ConditionsArchitectural Distortions Breast Tomosynthesis

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexFemale

AgeNot listed

SponsorM.D. Anderson Cancer Center

About this trial

To compare narrow-angle digital breast tomosynthesis (DBT) and wide-angle DBT.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women undergoing standard screening mammography.

Ability to understand and sign consent.

Disqualifiers

Pregnant women.

Women unable to consent.

Male patients.

Trial population

Screening mammography population at MD Anderson

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Digital Breast Tomosynthesis (DBT)
Device
Undergo tomosynthesis imaging

Treatment groups

100 Participants

are divided into 1 treatment group

Group A: Digital Breast Tomosynthesis (DBT)1 intervention

Trial outcomes

Primary outcomes

Safety and adverse events (AEs)

ncidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events

Time frame

Through study completion; an average of 1 year

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

M.D. Anderson Cancer Center

Lead sponsor

Siemens Medical Solutions

Collaborator

Source ClinicalTrials.gov

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