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OpenTrials
Completed

NCT Number: NCT04260620

Delphinus SoftVue™ ROC Reader Study (DMT SV RRS3)

The purpose of this multi-reader, multi-case (MRMC) reader study is to evaluate reader performance when SoftVue™ automated breast ultrasound and screening mammography are combined, compared to screening mammography alone, in women with dense breast parenchyma.

This reader study will include up to 32 radiologist readers and a sample of 140 breast screening cases that were selected from the library of images collected under Delphinus Protocol #DMT-2015.001 (NCT03257839) Arm 1 Phase B. The reader study image case set will be enriched with cancer cases.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Delphinus Medical Technologies, Inc.

Novi, Michigan, 48374, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Radiologists of any age, sex, race, ethnicity, or institutional affiliation may participate as study readers. All readers must meet the following base Inclusion Criteria:

  • Hold a current United States medical license
  • Be American Board of Radiology Certified
  • Be MQSA-qualified
  • Be experienced in reading DM images on a monitor
  • Be experienced in reading Breast Ultrasound images on a monitor
  • Have completed a Financial Disclosure showing no Conflicts of Interest
  • Have provided a current curriculum vitae (CV)
  • Have provided a signed Readers' Agreement
  • Have provided written Informed Consent

All qualified and confirmed readers will complete a multi-module SoftVue™ training program prior to their participation in a reading session for this study.

Treatment and study plan

Reading of Automated Breast Ultrasound in conjunction with Screening Mammography

Device

Reader performance when SoftVue automated breast ultrasound (SV) and digital screening mammography (DM) are combined, compared to screening mammography alone.

Other names: Digital Screening Mammography with Adjunctive SoftVue Screening Whole Breast Ultrasound

Primary outcomes

  1. MRMC Analysis: ROC AUC

    Time frame: 8 Weeks

    Area under the ROC curve (AUC)

Secondary outcomes

  1. Sensitivity and Specificity

    Time frame: 8 Weeks

    True Positive Rate and True Negative Rate

Sponsors and collaborators

Lead sponsor

Delphinus Medical Technologies, Inc.

Industry

Collaborators

  • Boston Biomedical Associates
  • University of Chicago

Registry information

Official study title

A Retrospective, Observational, Case-controlled, Multi-reader, Multi-case, Receiver Operating Characteristic (ROC) Study of Reader Performance When SoftVue Automated Breast Ultrasound (SV) and Digital Screening Mammography (DM) Are Combined, Compared to Screening Mammography Alone, in Asymptomatic Women With Heterogeneous or Extremely Dense Breast Parenchyma

Acronym: DMT SV RRS3

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Feb 7, 2020
Registry last updated
Feb 3, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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