High Intensity Focused Ultrasound Treatment of Breast Tumors. BRIFU Study

Recruiting · NCT03342625 · Interventional (participants receive a specific treatment)

Interventions studied

High Instensity Focused Ultrasound

Monocentric prospective study evaluating the efficacy of High intensity focused ultrasound (HIFU) in breast tumors.

Age range

18 Years and older

Sex

Female

Healthy volunteers

No - a diagnosis or condition is required

Phase

Not applicable (e.g. observational or device study)

Study type

Interventional (participants receive a specific treatment)

Histologically proven infiltrating ductal carcinoma with the analysis of hormone receptors, tumor grade, Her-2 expression.
T0 lesion, unifocal or plurifocal, with or without micro-calcifications associated, measuring 15 mm maximum major axis on ultrasound.
Clinical N0.
Bra cup size greater than or equal to B.
Markable and identifiable lesion in MRI.
Indication of partial or total mastectomy in case of multifocal lesions or extensive calcification associated with axillary surgery.
Breast assessment performed by a referent radiologist: Mammography, ultrasound, clinical examination.
No contraindication to MRI.

Infiltrating lobular carcinoma and Pure ductal carcinoma in situ.
Bilateral lesion.
Non-detectable MRI lesions, within 10 mm of the skin, greater than 15 mm on ultrasound.
Unifocal palpable tumor.
Cup size bra equal to A.
Cutaneous lesion on the breast to be treated by HIFU.
Impossibility of ventral decubitus immobility, extended arm, during 1 hour.
Pregnant or postpartum patient.
Patient participating in another interventional clinical trial within 30 days of enrollment and during the trial.

1 location listed.