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Clinical Trial NCT07487792 for Breast - Female is not yet recruiting. See the Trial Radar Card View and AI discovery tools for all the details. Or ask anything here. | ||
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Feasibility of Imaging Breast Implants With a Transmission-based Microwave Scanner 10
Clinical Trial NCT07487792 is an interventional study for Breast - Female and is currently not yet recruiting. Enrollment is planned to begin on 15 March 2026 and continue until the study accrues 10 participants. Led by University of Calgary, this study is expected to complete by 15 November 2026. The latest data from ClinicalTrials.gov was last updated on 23 March 2026.
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:
- Can a microwave imaging device effectively scan a breast containing implants?
- Can the presence of implants be identified in a microwave scan?
- Can the microwave...
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 ...
Show MoreOfficial Title
Feasibility of Imaging Breast Implants With a Transmission-based Transmission Scanner
Conditions
Breast - FemalePublications
Scientific articles and research papers published about this clinical trial:- Mojabi, Pedram, et al. "Feasibility of Tumor Detection with a Transmission-based Microwave Imaging System." Medical Physics (Lancaster), vol. 52, no. 9, 2025, pp. e18080-n/a, https://doi.org/10.1002/mp.18080.
- Mojabi, Pedram, et al. "Assessment of Breast Composition with A Transmission-Based Microwave Imaging System." IEEE Transactions on Biom...
Other Study IDs
- REB25-0914
NCT ID Number
Start Date (Actual)
2026-03-15
Last Update Posted
2026-03-23
Completion Date (Estimated)
2026-11-15
Enrollment (Estimated)
10
Study Type
Interventional
PHASE
N/A
Status
Not yet recruiting
Keywords
women
breast implant
breast implant
Primary Purpose
Other
Design Allocation
N/A
Interventional Model
Single Group
Masking
None (Open Label)
Arms / Interventions
| Participant Group/Arm | Intervention/Treatment |
|---|---|
ExperimentalA single arm study to determine feasibility of imaging breast implants WVI-MIS-03-2025 | WVI-MIS-03-2025 Microwave scans |
Primary Outcome Measures
Secondary Outcome Measures
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Measurement of regions of interest in microwave images | Images 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. | 12 months |
| Outcome Measure | Measure Description | Time Frame |
|---|---|---|
Comparison of total area in implant in microwave image with known physical size | The total area corresponding to the breast implant in the microwave images will be calculated and compared with the known implant size. | 12 months |
Compare microwave scans of the left and right breast | The properties and size of the region corresponding to the implant will be compared between right and left breasts. | 12 months |
Participation Assistant
Eligibility Criteria
Eligible Ages
Adult, Older Adult
Minimum Age
18 Years
Eligible Sexes
Female
- 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
- 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
Study Responsible Party
Elise Fear, Principal Investigator, Professor, University of Calgary
Study Central Contact
Contact: Anita Garland, 403-703-1664, [email protected]
Contact: Elise Fear, 403-210-5413, [email protected]
1 Study Locations in 1 Countries
Alberta
Demsey Plastic Surgery Clinic, Calgary, Alberta, T3H 3K8, Canada
Anita Garland, Contact, 403-703-1664, [email protected]