Breast 3DUS ABUS System Comparison

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWestern University, Canada

About this trial

This comparative study will recruit 30 females who are scheduled for mammography and ultrasound assessment. The clinical 2D ultrasound is performed routinely, and the research portion of this study will add a few extra 3-D ultrasound images during the procedure. The ultrasound imaging laboratory under the direction of Dr. Aaron Fenster has developed a customized device designed to acquire 3D ultrasound of the breast using a commercial ultrasound machine. The purpose is to see how well 3-dimensional ultrasound acquire from that device is able to visualize tumours and other key features in comparison to the clinical system InveniaTM developed by GE Medical.

Eligibility criteria

Qualifiers

Adult Patients who are scheduled for screening ABUS

Adults Patients who are scheduled for short term follow-up with ABUS.

Must be at least 18 years of age or older.

Must be proficient in English (reading/writing).

Disqualifiers

Patients with breast implants.

Patients with contraindication for ABUS.

Patients who cannot tolerate ABUS.

Trial design

Treatments tested in this trial

  • 3D Ultrasound Image Acquisition

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators