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Clinical Trial Summary

The primary hypothesis of this project is that using molecular breast imaging (MBI) in evaluating women with equivocal mammographic or sonographic findings will demonstrate high specificity in distinguishing benign from malignant breast disease and, as a result, decrease the number of biopsies.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT01687790
Study type Interventional
Source University of Pittsburgh
Contact
Status Completed
Phase N/A
Start date September 2012
Completion date September 2014

See also
  Status Clinical Trial Phase
Recruiting NCT01106911 - Assessment of Digital Breast Tomosynthesis (DBT) in the Screening Environment N/A
Active, not recruiting NCT02406274 - Use of Contrast Enhanced Spectral Mammography (CESM) for Women With Palpable Breast Abnormalities N/A
Terminated NCT00630318 - Testing New Method of Analyzing MR Images Phase 1
Completed NCT00722059 - Detection and/or Evaluation of Dense Breast Abnormalities Using Tomosynthesis and Digital Mammography Phase 0
Withdrawn NCT00722683 - Evaluate Breast Masses Using a New Method of Ultrasound Contrast to Detect Abnormal Blood Flow in Breasts N/A