Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Monteris Medical
This is a multicenter sub-study that will include comprehensive neuropsychological assessment data collection done at baseline (within 1 year prior to the index LITT procedure) and at follow-up (at least 6 months from the index LITT procedure). Visual field testing will be conducted in a subset of enrolled patients. Up to 250 subjects may be enrolled at up to 15 study sites.
Age
16–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
1. Patient or legally authorized representative provides written authorization and/or consent.
2. Patient is enrolled in the LAANTERN trial and had an epilepsy diagnosis without the presence of a malignant brain tumor.
3. Patient is 16 years of age or older.
4. Patient has completed a baseline comprehensive neuropsychological assessment with a neuropsychologist.
You may not be if
1\. Patient does not complete the index LITT procedure as specified in the LAANTERN registry.
Clareo Health | PatiEnt Neuropsychological outcomeS After laseR Ablation
