Augmented Reality Feasibility for Non-invasive Preoperative Tracking in Breast Cancer Surgery
Recruiting
N/A
Interventional Study
Subclinical Breast Cancer Lesion
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 100
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 20 (estimated)
- Sponsor
- Centre Jean Perrin · Other
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About This Trial
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: radi…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Major women
* Requiring conservative surgical management of a subclinical cancerous breast lesion (not palpable), the histology of which has been previously proven by anatomopathology;
* Having a breast MRI indication at the time of the breast assessment performed at the Centr…
Contacts
Dr Sabrina MADAD-ZADEH
0473278005
CONTACT