To determine if the Clarity 3DUS (3D Ultrasound) system can be used by multiple individuals
to acquire 3DUS images and produce consistent TB (Tumor Bed) shifts for breast IGRT
(Image-Guided Radiation Therapy).
Procedure: Image-Guided Radiation Therapy using 3D Ultrasound Guided-Therapy
Procedure: Ultrasound Guided Imaging
Procedure: 3 DUS
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Full eligibility criteria for NCT00911456
Ages eligible for Study
18 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
Subjects will be 27 consenting women undergoing CT simulation for adjuvant breast radiotherapy at VIC ≤16 weeks after BCS.
Women must have primary tumors <3cm, pathologically N0 disease, and negative surgical margins.
Seroma clarity score <2
Patients will be excluded if they have had mastectomy or receive adjuvant chemotherapy that results in the CT simulation session occurring >16 weeks after the BCS date.
All locations for NCT00911456
BC Cancer Agency Vancouver Island BCCA
Victoria, British Columbia, Canada, V8R 6V5
View full eligibility
Tris trial is registered with FDA with number: NCT00911456. The sponsor of the trial is British Columbia Cancer Agency and it is looking for 27 volunteers for the current phase.
Official trial title: Can 3D Ultrasound Be Used Reproducibly by Radiation Therapists in Partial Breast Image-Guided Radiation Therapy?
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