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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00723541
Other study ID # HUM 00003483
Secondary ID 5R01CA151443-05
Status Completed
Phase N/A
First received
Last updated
Start date January 2008
Est. completion date July 12, 2016

Study information

Verified date January 2020
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to develop a computer-aided diagnosis system to find breast lesions, including masses and microcalcifications, which hopefully will improve breast cancer detection and classification.


Description:

The purpose of this study is to develop a computer-aided diagnosis system to find breast lesions, including masses and microcalcifications, and determine if the lesion is a cancer or not for digital tomosynthesis mammography (DTM).


Recruitment information / eligibility

Status Completed
Enrollment 872
Est. completion date July 12, 2016
Est. primary completion date July 12, 2016
Accepts healthy volunteers No
Gender Female
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Subjects scheduled for core biopsy of a breast lesion

Exclusion Criteria:

- Pregnant females

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Computer aided analysis of breast lesions
Tomosynthesis mammography and computer aided analysis of breast lesions to aid in detection of breast cancer.

Locations

Country Name City State
United States University of Michigan Health System Ann Arbor Michigan

Sponsors (2)

Lead Sponsor Collaborator
University of Michigan National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Achieve earlier breast cancer detection and characterization 1 year
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