Confocal Histolog Scanner in Routine Breast-Conserving Surgery (CHiB)
Recruiting
N/A
Interventional Study
Breast Cancer Invasive
Breast Cancer Surgery
Lumpectomy
Confocal Laser Endomicroscopy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 100 (estimated)
- Sponsor
- University of Fribourg · Other
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About This Trial
The clinical performance study is collecting data from the use of a CE mark product used within the scope of its intended purpose to intraoperatively visualize tissue specimen. The subjects are not submitted to invasive and burdensome procedures compared to the standard of care surgical practices and regular use of the CE mark product.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult female Subject ≥18 years old.
* Subject scheduled for breast conserving surgery of invasive and/or in-situ ductal and lobular carcinoma.
* Subject is able to read, understand and sign the informed consent.
Exclusion Criteria:
* Subject with planned mastectomy
* Subject…
Contacts
No contact information available.