Actively Recruiting
Augmented Reality Feasibility for Non-invasive Preoperative Tracking in Breast Cancer Surgery
Led by Centre Jean Perrin · Updated on 2025-12-31
20
Participants Needed
1
Research Sites
158 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Breast cancer is diagnosed by imaging at a non-palpable stage in more than half of all cases. Surgical removal requires preoperative guidance. Generally, preoperative guidance is performed using a metal guide under local anaesthetic and radiological control. This type of guidance has several limitations. For the patient, it can be painful and traumatic. The procedure involves two departments: radiology and the operating theatre, which poses logistical constraints. What's more, between 10% and 40% of patients require repeat surgery for unhealthy margins, raising the question of the effectiveness of the tracking procedure. The investigators propose to develop a non-invasive intraoperative guidance system: Augmented Reality, which will provide a 3D vision with virtual transparency of the breast during surgery, thanks to real-time fusion of preoperative imaging with video from a camera located in the operating room. The process is illustrated below. Illustration of the general principle of the augmented reality system for locating non-palpable breast lesions. The images above represent a preliminary test carried out on the computer outside the operating room. This is an initial research prototype which has not yet been validated and is not suitable for routine use.
CONDITIONS
Official Title
Augmented Reality Feasibility for Non-invasive Preoperative Tracking in Breast Cancer Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female adults
- Require conservative surgery for a non-palpable breast cancer lesion confirmed by pathology
- Have a breast MRI indicated during assessment at Centre Jean Perrin
- Able to give informed consent
- Registered with a social security scheme
You will not qualify if you...
- Breast cancer during pregnancy
- Under guardianship, deprived of liberty, or unable to consent
- Decline to participate
AI-Screening
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Trial Site Locations
Total: 1 location
1
Centre Jean PERRIN
Clermont-Ferrand, France, 63011
Actively Recruiting
Research Team
C
Céleste PINARD
CONTACT
D
Dr Sabrina MADAD-ZADEH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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