Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
FEMALE
NCT06512558

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

Age: 18Years - 100Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Centre Jean PERRIN

Clermont-Ferrand, France, 63011

Actively Recruiting

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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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