Study of ExAblate Focused Ultrasound Ablation of Breast Cancer
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|ClinicalTrials.gov Identifier: NCT01620359|
Recruitment Status : Completed
First Posted : June 15, 2012
Last Update Posted : August 31, 2016
The goal of this prospective, non-randomized, single-arm, multi site, international study is to develop data to evaluate the safety and effectiveness of the ExAblate MRgFUS system in the ablation of breast cancer and of MRI.
The goal of MRgFUS ablation of breast cancer is to plan and ablate the entire tumor volume in a treatable and device accessible location.
|Condition or disease||Intervention/treatment||Phase|
|Breast Cancer||Device: ExAblate MRgFUS||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||14 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Study of ExAblate Focused Ultrasound Ablation of Breast Cancer Under MR Guidance (MRgFUS) and MRI Evaluation of Ablation|
|Study Start Date :||June 2011|
|Actual Primary Completion Date :||July 2016|
|Actual Study Completion Date :||July 2016|
Device: ExAblate MRgFUS
100% ablation of an up-to-2-cm breast cancer visible on an contrast-enhanced MRI with 5-10 mm margins around the primary tumor
- Adverse Events [ Time Frame: 5 weeks post treatment ]To evaluate the incidence and severity of the ExAblate MRgFUS device-related complications to establish the safety profile of the ExAblate ablation of breast cancer visible on contrast-enhanced MRI with 5-10 mm margins around the primary tumor
- Histopathological analyses [ Time Frame: 5 weeks post treatment ]To estimate the effectiveness of ExAblate MRgFUS to ablate 100% of an up-to-2-cm breast cancer visible on an contrast-enhanced MRI with 5-10 mm margins around the primary tumor.
- MR imaging [ Time Frame: 5 weeks post treatment ]To estimate the sensitivity of post-ablation MRI in identifying residual disease following ablation.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01620359
|Bottrop, Germany, 46236|
|Principal Investigator:||Hans Kolberg, MD||FUS BOTTROP|