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Evaluation of the Efficacy of Digital Breast Tomosynthesis Imaging

NCT01373671 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 764

Last updated 2020-08-07

Study results available
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Summary

The primary objective of this protocol is to collect the 2-dimensional (2D) screening and diagnostic images, and 3-dimensional (3D) Digital Breast Tomosynthesis (DBT) scans from patient mammography examinations acquired on various commercially available Full Field Digital Mammography (FFDM) systems and the Siemens Inspiration DBT system, respectively.

Conditions

Interventions

DEVICE

SIEMENS INSPIRATION DIGITAL BREAST TOMOSYNTHESIS (DBT) SYSTEM

DBT scan

Sponsors & Collaborators

  • Siemens Medical Solutions USA - CSG

    lead INDUSTRY

Principal Investigators

  • Agnes Lazar · Siemens Medical Solutions USA, Inc

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2014-05-31
Completion
2014-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01373671 on ClinicalTrials.gov