PREselection of patients at risk for COgnitive DEcline after Radiotherapy using advanced MRI (PRECODE-MRI)
- Conditions
- benignbrain tumourMeningioma10029209
- Registration Number
- NL-OMON52049
- Lead Sponsor
- MAASTRO clinic
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 67
- Meningioma WHO I, grading based on pathology or radiological features
- Age >= 18 years.
- Karnofsky Performance Score 70 or above.
- Ability to comply with the protocol, including neuropsychological testing and
imaging.
- Ability to understand the requirements of the study and to give written
informed consent, as determined by the treating physician.
- Written informed consent.
- Resection meningioma < 3mnd
- Age < 18 years
- Pregnancy
- Any prior cranial radiotherapy
- Any prior chemotherapy in the last 5 years
- Contra-indication for MR imaging (i.e. metal implants, claustrophobia)
- Any other serious medical condition that could interfere with follow-up.
- Severe aphasia or language barrier interfering with assessing endpoints (i.e.
completion of questionnaires or neurocognitive performance)
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Correlation between the delta cognitive failure score (baseline vs 2 years) and<br /><br>radiotherapy dose in cognition related brain regions (supratentorial brain,<br /><br>hippocampus left/right and anterior/posterior, cerebellum anterior/posterior).</p><br>
- Secondary Outcome Measures
Name Time Method