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| ID | Type | Description | Link |
|---|---|---|---|
| ID-RCB number : 2017-A01490-53 | Other Identifier | ANSM |
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| Name | Class |
|---|---|
| Ligue contre le cancer, France | OTHER |
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Monocentric prospective study evaluating the efficacy of High intensity focused ultrasound (HIFU) in breast tumors.
Incidence of breast cancer increases with the lifetime of the population, and represents an important socio-economic issue. Diagnosis and treatment are major public health issues. High Instensity Focused Ultrasound (HIFU) is a minimally invasive technique which decreases the risk of post-treatment complications and allows shorter hospitalization times. This technology is also remarkable for the absence of limitation related to the dose delivered, which makes it possible to repeat if necessary and the absence of ionizing radiation both for the treatment itself and for its guidance (MRI).
The main objective is to evaluate the efficacy of HIFU for the treatment of breast tumors, based on histological criteria.
Indication :
Histologically invasive ductal carcinoma, T0, with unifocal or plurifocal lesion, with or without associated microcalcifications, measuring 15 mm maximum on ultrasound and clinical N0.
Course of the study :
Number of patients :
15 patients will be included in this pilot study. If no success is observed, the study will be stopped and the technique considered inefficient. If there are one or more successes, an Independant Data Monitoring Committee (IDMC) will meet to propose an additional trial if necessary with the data from this trial.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| High Intensity Focused Ultrasound | Experimental | High Intensity Focused Ultrasound for the treatment of breast tumors, guided by MRI |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| High Instensity Focused Ultrasound | Device | High Intensity Focused Ultrasound guided by MRI |
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| Measure | Description | Time Frame |
|---|---|---|
| Efficacy of HIFU for the treatment of breast tumors, based on histological criteria |
| Day 30 |
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility of non-invasive pre-surgical identification of the tumor area to be resected (palpation by the surgeon of the focused ultrasound ablation zone) | Day 2, 8 | |
| Immediate complications of focused ultrasound | Day 30 |
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Inclusion Criteria :
Exclusion Criteria :
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jean PALUSSIERE, MD | Contact | +33 5 56 33 37 50 | j.palussiere@bordeaux.unicancer.fr | |
| Simone MATHOULIN-PELISSIER, MD, PhD | Contact | s.mathoulin@bordeaux.unicancer.fr |
| Name | Affiliation | Role |
|---|---|---|
| Jean PALUSSIERE, MD | Institut Bergonié | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institut Bergonie | Recruiting | Bordeaux | 33076 | France |
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| Pain (visual analogue scale) experienced by patients during the sedation procedure, until surgery. | Day 0, 2 |