Clinical trial · Interventional
Safety and Effectiveness of MR Guided Focused Ultrasound Surgery in the Treatment of Early Breast Carcinomas
A Clinical Study To Evaluate the Safety and Effectiveness of MR Guided Focused Ultrasound Surgery in the Treatment of Early Breast Carcinomas
NCT02794558CI-TRIAL-00039277completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 9, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260909-000002
Summary
Brief summary (as posted)
Non-randomized, Single Arm Clinical study to Evaluate the Safety and Effectiveness of MR Guided Focused Ultrasound Surgery in the Treatment of Early Breast Carcinomas
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ExAblate MRgFUS | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment Arm
- description
- Subjects in this arm are treated once with MRgFUS device
- interventionNames
- Device: ExAblate MRgFUS
Primary outcomes (1)
- measure
- Incidence and severity of Adverse events
- timeFrame
- 5 years
- description
- Safety of the treatment will be evaluated by recording and assessing the incidence and severity of device- related complications
Secondary outcomes (1)
- measure
- Post treatment local recurrence
- timeFrame
- 5 years
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Women age ≥ 18 years with - breast cancer proven by 14-20 G. core needle biopsy of the breast lesion. * No evidence of cancer at the sentinel/ Axillary node * Women in whom breast MR imaging identifies a single focal well-demarcated breast lesion less than or equal to 1.5 cm in diameter with stage T1, N0, M0 disease. * Patient received neoadjuvant care for 4 weeks such as: Hormone replacement therapy or Tamoxifen is permissible where the tumor is less than or equal to 1.5 before neoadjuvant therapy * Able and willing to give consent and able to attend all study visits. * Able to communicate sensations during the MRgFUS procedure. * Life expectancy of 5 years or more. Exclusion Criteria: * Breast cancer which was diagnosed by incisional / excisional biopsy * Contraindication to MRI (non-MRI compatible implanted metal devices). * Pregnant or lactating post partum women. * Prior XRT or laser or cryo-therapy to the target breast. * Difficulty lying prone and still for up to 210 minutes in the MR unit, e.g., COPD, heart disease, lung disease, sleep apnea or airway problems, severe asthma, severe arthritis, severe claustrophobia. * Patients with unstable cardiac status including: * Unstable angina pectoris on medication. * Patients with documented myocardial infarction within six months of protocol entry. * Congestive heart failure requiring medication. * Patients on anti-arrhythmic drugs. * Severe hypertension (diastolic BP \> 100 on medication). * Patients with cardiac pacemakers. * Immunosuppressed patients, e.g., patients receiving steroids or other immunosuppressive medication, insulin-dependent diabetes mellitus, collagen vascular disease. * Patients receiving chemotherapy * Patients with history of grand mal seizures, severe cerebrovascular disease (multiple CVA or CVA within 6 months), hemolytic anemia (hematocrit \< 30), or patients on dialysis. * Patients currently receiving anticoagulation therapy. * Large patients who cannot fit comfortably in the magnet, or patients \> 100Kg. * Lesions difficult to target (\<1 cm from skin, nipple-areola complex or the ribcage), as visualized on pre-therapy MRI. * Microcalcifications as the only sign of breast cancer on imaging studies. * Patients with breast implants. * Prior reaction to gadolinium-based contrast agent * Prior radiation to the breast, which is about to be treated. * Evidence of tumor at any location other then the targeted lesion. * Histological type of invasive micropapillary carcinoma because of cancer displacement by the needle * Mucinous carcinoma which was diagnosed by core needle biopsy because of needle cancer displacement
References
Publications (0)
Data not yet available
No reference posted for this study.