Transcutaneous Breast Cancer Diagnosis by Canine Odorology

STATUS

Recruiting
participants needed

450
sponsor

Institut Curie

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Updated on 19 February 2024

See if I qualify

insulin

corticosteroids

fever

breast carcinoma

carcinoma

cancer diagnosis

breast imaging reporting and data system

ultrasound breast

Summary

Patient with an indication of interventional percutaneous procedure for characterization of a breast lesion, palpable or not, classified as category 4 or 5, according to the Breast Imaging (BI) Report and Data System of the American College of Radiology (RADS) classification detected at mammography and/or breast ultrasound examination.

Details

Condition	Breast Cancer, Breast Cancer
Age	18-100 years
Treatment	Odour sampling
Clinical Study Identifier	NCT04217109
Sponsor	Institut Curie
Last Modified on	19 February 2024

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Eligibility		Yes	No	Not Sure
Inclusion Criteria
	Women 18 years and older, with one or more ipsilateral mammary lesion(s), palpable or not, detected at mammography and/or ultrasound and with at least one lesion classified as BI-RADS category 4 or 5 with an indication of percutaneous sampling (cytology, microbiopsies, macro-biopsies)
	Benefit from the national social security
	Signature of the informed consent of the study
	There is no contraindication for the person to simultaneously participate to another research program and there is no exclusion period planned after the study
Exclusion Criteria
	Patient with bilateral breast lesions classified as BI-RADS category 4 or 5
	Patient with breast implant(s)
	Patient with a personal history of breast surgery for benign lesion(s) of the concerned breast operated less than 4 weeks before the date of inclusion in this study
	Patient with a personal history of cancer (in situ or invasive) less than 5 years before inclusion whatever the anatomical site including cutaneous basal cell carcinoma
	Patient with a personal history of punctures and/or percutaneous breast biopsies of the concerned breast less than 4 weeks before inclusion
	Patient with a breast skin ulceration
	Patient under insulin (risk of sudation that may impair compress sample)
	Concomitant antibiotics or corticoids taken one week before inclusion in the study
	Patient with a current viral infection (fever)
	Persons under guardianship or deprived of liberty
	Impossibility to submit to the medical monitoring expected by the study for geographical or severe psychological reasons

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Transcutaneous Breast Cancer Diagnosis by Canine Odorology