This is an open label, single arm, prospective, and pilot study. Eligible patients will be enrolled after acquiring the signed informed consent and then will receive the treatment of re-RT combined with FUS (FUS + re-RT) on an outpatient basis. The re-RT in FUS + re-RT treatment will include fractioned stereotactic radiosurgery (SRS) treatment (FUS + SRS) or conventional radiotherapy (cRT) treatment (FUS + cRT). The treatment of SRS or cRT treatment given to patients is determined by the investigator depending on the volume and location of the treatment region.
Condition | Recurrent Glioblastoma |
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Treatment | NaviFUS System |
Clinical Study Identifier | NCT04988750 |
Sponsor | NaviFUS Corporation |
Last Modified on | 28 January 2023 |
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