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Low Dose Tomosynthesis Compared to Traditional Tomosynthesis

NCT02771444 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2018-03-26

No results posted yet for this study

Summary

This study aims to evaluate image quality of a low-dose tomosynthesis system versus a comparator. Subjects will undergo a four-view tomosynthesis examination with the comparator and with the study device, and images will be assessed by several radiologists by comparing details in the images from the two systems.

Conditions

  • Breast Neoplasms

Interventions

DEVICE

Tomo Assessment

A four-view tomosynthesis examination

Sponsors & Collaborators

  • Philips Digital Mammography Sweden AB

    lead INDUSTRY

Principal Investigators

  • Pietro Panizza, M.D · Ospedale San Raffaele

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-31
Primary Completion
2018-03-22
Completion
2018-03-22

Countries

  • Italy

Study Locations

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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 NCT02771444 on ClinicalTrials.gov