Brain metastases brain tumours
Conditions
Interventions
None listed
Sponsors
Antoni van Leeuwenhoek Ziekenhuis
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Patient must be planned for mask based or frame based SRS on the ICON system at our institute Patients/Volunteers must be 18 years or older Patients/Volunteers must sign informed consent
Exclusion criteria
Exclusion criteria: A contra-indication for use of the Elektromagnetic tracking system, e.g. a pacemaker.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The correlation between nose-tip motion and position with respect to motion and position of the head of the subject. Per fraction we will have at least 18000 measurements (30 minutes x 10 Hz) based on which we can build a correlation model. Based on the EM tracking system and the CBCT data we can calculate the actual tumour displacement during a fraction. For different thresholds of actual tumour motion (0.5 mm, 1 mm, 1.5 mm, and 2 mm) we will establish the needed threshold for the HDMM system, and its accuracy in detecting the motion. | — |
Secondary
| Measure | Time frame |
|---|---|
| The immobilization capabilities of the different masks will be assessed as the position and orientation deviation of the three sensors on the head in time with respect to the first measurement using a rigid point match. The comfort of the different masks will be assessed based on scoring of the volunteers. For each mask they will score the comfort on a scale of 1 to 10. Data will be evaluated in a paired manor as this is observer dependent. | — |
Countries
Netherlands
Outcome results
None listed