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Feasibility of Imaging Breast Implants With a Transmission-based Microwave Scanner

Feasibility of Imaging Breast Implants With a Transmission-based Transmission Scanner

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07487792
Enrollment
10
Registered
2026-03-23
Start date
2026-09-15
Completion date
2026-12-30
Last updated
2026-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast - Female

Keywords

women, breast implant

Brief summary

The goal of this clinical trial is to assess whether microwave scans can depict the presence of implants in the breast in women with existing breast implants that were surgically placed at least 6 months ago. The main questions it aims to answer are: 1. Can a microwave imaging device effectively scan a breast containing implants? 2. Can the presence of implants be identified in a microwave scan? 3. Can the microwave scans of the left and right breasts be compared to assess whether similarity is observed?

Detailed description

Breast implants are consistently one of the top 5 cosmetic procedures performed each year in North America. The Food and Drug Administration (FDA) cites a 10% risk of rupture over 10 years (1% cumulative per annum risk of device rupture). Rupture refers to disruption in the integrity of the implant, and is typically age-related deterioration where age in this context refer to the implant. Rupture in saline implants is detected with rapid change in breast size. With silicone implants, rupture is much more challenging to detect as it is rare to have a completely collapsed implant shell. Current recommendations for surveillance of breast implants include Magnetic Resonance Imaging (MRI) or ultrasound within 5-6 years of surgery for the initial test, then every 2-3 years. The guideline initially included only MRI but was adjusted in 2022 to include ultrasound. Patient adherence to guidelines with only MRI was very low (less than 5%), which is postulated to relate to the expense, discomfort, and inaccessibility of MRI. Mammography is a frequently used breast imaging method. However, the majority of women with implants are too young for breast screening programs that involve regular mammograms. Also, the implant is displaced during mammography to focus on the breast tissues. Finally, mammography involves exposure to x-rays, limiting regular scans in women too young for screening. Therefore, there is a need to regularly inspect silicone implants for silent rupture. An imaging approach that is low-cost, available at point-of-care, easy to use, and reliable (i.e. sensitive to implant rupture) would be a valuable tool for plastic surgery clinics. Microwave imaging has been proposed as a low-cost and comfortable approach to breast imaging that can be performed at point of care. This approach to imaging is low power, so no tissue heating occurs and there are no other side effects. Therefore, microwave imaging is suited to in-clinic, ongoing monitoring of the breast. 10 women with breast implants will be recruited from plastic surgery clinics. This includes women with breast implants that were surgically placed at least 6 months prior and are asymptomatic for implant rupture, as well as women who have implants with a confirmed rupture. Study participants will be scanned with the microwave imaging system. Three scans of each breast will be collected in each of the Craniocaudal (CC) and Mediolateral Oblique (MLO) views. The breast positioning will be adjusted between scans to maximize the presentation of the implant in the imaging volume. The images will be analyzed to identify the implants, as the implants have different properties when compared to healthy breast tissues.

Interventions

DEVICEWVI-MIS-03-2025

Microwave scans

Sponsors

University of Calgary
Lead SponsorOTHER
Wave View Imaging Inc.
CollaboratorUNKNOWN

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women with breast implants placed at least 6 months prior who are asymptomatic for implant rupture as well as those with known implant rupture * Female * Minimum of 18 years of age * Able to provide informed consent

Exclusion criteria

* Women who are currently pregnant or breastfeeding * Women with active breast infections * Women with nipple piercings (unless removed prior to scanning) * Women with implanted electronic device * Women with physical limitations that prevent them from placing their breasts inside the scanner

Design outcomes

Primary

MeasureTime frameDescription
Measurement of regions of interest in microwave images12 monthsImages of both breasts will be created. Regions of interest corresponding to the breast implants will be identified using the electrical properties. The size of these regions will be calculated.

Secondary

MeasureTime frameDescription
Comparison of total area in implant in microwave image with known physical size12 monthsThe total area corresponding to the breast implant in the microwave images will be calculated and compared with the known implant size.
Compare microwave scans of the left and right breast12 monthsThe properties and size of the region corresponding to the implant will be compared between right and left breasts.

Countries

Canada

Contacts

CONTACTAnita Garland
anita.garland@ucalgary.ca403-703-1664
CONTACTElise Fear
fear@ucalgary.ca403-210-5413

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 26, 2026