Acute electrocorticographic signal recording at the operating room
- Conditions
- A, this is basic brain function researchNA
- Registration Number
- NL-OMON48449
- Lead Sponsor
- eurology & Neurosurgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 84
- age 18 years and higher and mentally competent;
- a clinical indication for resection of a tumor or other lesion (e.g. focus of
epileptic seizures);
- a clinical indication for awake surgery (or if applicable, for a full asleep
procedure);
- indication for longer than average (225 min) duration of the procedure
(estimation by the neurosurgeon);
- the neurosurgeon decides that a certain patient is not eligible to
participate in the study (e.g. for medical or surgical reasons);
- planned trepanation too far away for grid placement on a target location
(evaluation by the neurosurgeon and researcher combined);
- reported function loss that prohibits the accurate performance of the
required tasks;
Other exclusion criteria refer to specific parts of the study and do not affect
the overall exclusion of the study. These are for example exclusion criteria
for fMRI research, which include pregnancy, claustrophobia and presence of
metals in the body
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The end-points per primary objective are as follows:<br /><br>1) Achieving offline high-dimensional BCI control using high-density ECoG grids.<br /><br>2) Establishing and modeling of the relationship between hemodynamic signals<br /><br>measured with fMRI or optical imaging and the underlying neuronal activation<br /><br>patterns measured with high-density ECoG.</p><br>
- Secondary Outcome Measures
Name Time Method <p>NA</p><br>