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Ultrasound Imaging Technique in Detecting Breast Microcalcifications in Patients Undergoing Biopsy for a Breast Abnormality

Primary Purpose

Breast Carcinoma, Microcalcification

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Ultrasound
MicoPure ultrasound
Biopsy of Breast
Sponsored by
Sidney Kimmel Cancer Center at Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Breast Carcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Give written informed consent
  • Be scheduled for a sonographic or stereotactic guided core needle biopsy or surgical excision for the evaluation of a breast lesion or abnormality containing microcalcifications seen on mammography

Exclusion Criteria:

  • Is clinically unstable, severely ill, or moribund

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Diagnostic (standard ultrasound, MicroPure, biopsy)

    Arm Description

    Patients undergo grayscale and MicroPure ultrasound imaging followed by sonographic or stereotactic guided core needle biopsy or surgical resection. Surgical specimens are then x-rayed.

    Outcomes

    Primary Outcome Measures

    Number of microcalcifications seen on MicroPure ultrasound
    The number of microcalcifications seen on MicroPure ultrasound will be recorded and compared to x-ray imaging of the area undergoing the biopsy procedure (as the reference standard). The difference in agreement between the two ultrasound modes (relative to mammography) will be assessed using McNemar's test for correlated proportions, where p-values less than 0.05 are considered significant. A dichotomous parameters indicating agreement with mammography with respect to the exact number of microcalcifications (as yes or no) will be calculated and compared.
    Number of microcalcifications seen on grayscale ultrasound
    The number of microcalcifications seen on grayscale ultrasound will be recorded and compared to x-ray imaging of the area undergoing the biopsy procedure (as the reference standard). The difference in agreement between the two ultrasound modes (relative to mammography) will be assessed using McNemar's test for correlated proportions, where p-values less than 0.05 are considered significant. A dichotomous parameters indicating agreement with mammography with respect to the exact number of microcalcifications (as yes or no) will be calculated and compared.

    Secondary Outcome Measures

    Number of microcalcifications determined by pathology findings
    The results of the three imaging methods will be compared to the pathology findings using the American College of Radiology Breast Imaging Reporting and Data System lexicon for the assessment of breast lesions.

    Full Information

    First Posted
    January 20, 2017
    Last Updated
    November 13, 2017
    Sponsor
    Sidney Kimmel Cancer Center at Thomas Jefferson University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03031561
    Brief Title
    Ultrasound Imaging Technique in Detecting Breast Microcalcifications in Patients Undergoing Biopsy for a Breast Abnormality
    Official Title
    Breast Microcalcifications Identified With MicroPure as a Marker for Malignancy Compared to Grayscale Ultrasound and Mammography (Using Biopsy as the Reference Standard)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    March 1, 2012 (Actual)
    Primary Completion Date
    April 30, 2015 (Actual)
    Study Completion Date
    March 10, 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Sidney Kimmel Cancer Center at Thomas Jefferson University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This clinical trial studies a new type of ultrasound technique, MicroPure, in detecting breast microcalcifications in patients undergoing biopsy for a breast abnormality. Ultrasound sends sound waves into the body, and the sound waves reflected back are interpreted by the machine into a grayscale image. MicroPure uses a filter that adjusts the brightness and gives color to the ultrasound images, which may allow doctors to better identify microcalcifications. Microcalcifications are tiny deposits of calcium in the breast that cannot be felt but can be detected by imaging. A group of microcalcifications may indicate that cancer is present.
    Detailed Description
    PRIMARY OBJECTIVES: I. Evaluate MicroPure relative to grayscale ultrasound imaging for the identification of microcalcifications with mammography as the reference standard. SECONDARY OBJECTIVES: I. Evaluate MicroPure compared to grayscale ultrasound imaging and mammography for the characterization of breast abnormalities associated with microcalcifications using biopsy results as the reference standard (sensitivity and specificity will be calculated). II. Evaluate MicroPure relative to specimen x-ray imaging for the identification of breast microcalcifications with pathology as the reference standard. III. Estimate the improvements in patient care that may be achievable if MicroPure guided core needle biopsy procedures can replace some surgical excisions for the evaluation of breast abnormalities.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Breast Carcinoma, Microcalcification

    7. Study Design

    Primary Purpose
    Screening
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    85 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Diagnostic (standard ultrasound, MicroPure, biopsy)
    Arm Type
    Experimental
    Arm Description
    Patients undergo grayscale and MicroPure ultrasound imaging followed by sonographic or stereotactic guided core needle biopsy or surgical resection. Surgical specimens are then x-rayed.
    Intervention Type
    Device
    Intervention Name(s)
    Ultrasound
    Other Intervention Name(s)
    Ultrasound Imaging, US
    Intervention Description
    Undergo standard ultrasound
    Intervention Type
    Device
    Intervention Name(s)
    MicoPure ultrasound
    Intervention Description
    Undergo MicoPure ultrasound
    Intervention Type
    Procedure
    Intervention Name(s)
    Biopsy of Breast
    Other Intervention Name(s)
    Breast Biopsy
    Intervention Description
    Undergo breast biopsy or surgical resection
    Primary Outcome Measure Information:
    Title
    Number of microcalcifications seen on MicroPure ultrasound
    Description
    The number of microcalcifications seen on MicroPure ultrasound will be recorded and compared to x-ray imaging of the area undergoing the biopsy procedure (as the reference standard). The difference in agreement between the two ultrasound modes (relative to mammography) will be assessed using McNemar's test for correlated proportions, where p-values less than 0.05 are considered significant. A dichotomous parameters indicating agreement with mammography with respect to the exact number of microcalcifications (as yes or no) will be calculated and compared.
    Time Frame
    Baseline
    Title
    Number of microcalcifications seen on grayscale ultrasound
    Description
    The number of microcalcifications seen on grayscale ultrasound will be recorded and compared to x-ray imaging of the area undergoing the biopsy procedure (as the reference standard). The difference in agreement between the two ultrasound modes (relative to mammography) will be assessed using McNemar's test for correlated proportions, where p-values less than 0.05 are considered significant. A dichotomous parameters indicating agreement with mammography with respect to the exact number of microcalcifications (as yes or no) will be calculated and compared.
    Time Frame
    Baseline
    Secondary Outcome Measure Information:
    Title
    Number of microcalcifications determined by pathology findings
    Description
    The results of the three imaging methods will be compared to the pathology findings using the American College of Radiology Breast Imaging Reporting and Data System lexicon for the assessment of breast lesions.
    Time Frame
    Baseline

    10. Eligibility

    Sex
    Female
    Gender Based
    Yes
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Give written informed consent Be scheduled for a sonographic or stereotactic guided core needle biopsy or surgical excision for the evaluation of a breast lesion or abnormality containing microcalcifications seen on mammography Exclusion Criteria: Is clinically unstable, severely ill, or moribund
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Flemming Forsberg, PhD
    Organizational Affiliation
    Sidney Kimmel Cancer Center at Thomas Jefferson University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Links:
    URL
    http://hospitals.jefferson.edu/
    Description
    Thomas Jefferson University Hospital

    Learn more about this trial

    Ultrasound Imaging Technique in Detecting Breast Microcalcifications in Patients Undergoing Biopsy for a Breast Abnormality

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