Geen specifieke aandoening te benoemen. De ontwikkelde protocollen en beeldverwerkingstechnieken kunnen voor verschillende aandoeningen worden gebruikt. protocol development
Conditions
Interventions
None listed
Sponsors
Universitair Medisch Centrum Utrecht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria:, - >= 18 years - Capable and prepared to sign informed consent - Healthy volunteers or cancer patients who will be or are treated at the radiotherapy department, or patients with cancer at a stage or at a site that is not routinely treated with radiotherapy, where the aim is that future patients with a similar tumor stage or tumor site might be treated on the MRL.
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study:, - Contraindication for MRI scanning as listed in screening form - Neurological or psychiatric diagnosis - MRI contraindications such as (possible) pregnancy and metal or electronic implants not compatible with MRI - Refusal of subjects to be informed of chance findings possibly relevant to their health - In case study participation would interfere with regular treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The optimized MRI protocols and processing techniques required for MRI guided radiotherapy on the MR linac measured as signal to noise ratio, contrast, and acquisition time. | — |
Countries
Netherlands
Contacts
Public ContactM. Intven
Universitair Medisch Centrum Utrecht
Outcome results
None listed