This study evaluates the efficacy of the HIFU for the treatment of breast fibroadenoma with the FastScan version using assessment of patient experience and adverse event reporting.
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Number of participants with adverse events
Timeframe: 1 day post treatment
Number of participants with adverse events
Timeframe: 3 days post treatment
Number of participants with adverse events
Timeframe: 7 days post treatment
Change from Baseline volume of the fibroadenoma at 6 months
Timeframe: 6 months post treament
Change from Baseline Patient pain intensity score (100mm visual analog scale) at 1 day
Timeframe: 1 day post treatment
Change from Baseline Patient pain intensity score (100mm visual analog scale) at 3 days
Timeframe: 3 days post treatment
Change from Baseline Patient pain intensity score (100mm visual analog scale) at 7 days
Timeframe: 7 days post treatment
Patient satisfaction questionnaire
Timeframe: 6 months post treatment