A Pilot Study - Comparison of Two Hologic 3D Mammography Systems

NCT00759447 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 240

Last updated 2019-02-22

No results posted yet for this study

Summary

Study to compare the prototype tomosynthesis mammography system to the tomosynthesis system slated for commercial release.

Conditions

Interventions

DEVICE

Genesis and Gemini

3 dimensional breast mammography system

DEVICE

Investigational 3D Mammography system

3 dimensional breast mammography system

Sponsors & Collaborators

  • Hologic, Inc.

    lead INDUSTRY

Eligibility

Min Age
30 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2008-09-30
Completion
2008-09-30
FDA Device
Yes

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Entities

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 NCT00759447 on ClinicalTrials.gov