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.
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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

Céleste PINARD

0473278005

Celeste.PINARD@clermont.unicancer.fr

CONTACT

Dr Sabrina MADAD-ZADEH

0473278005

CONTACT