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Exploring the Neural Basis of Cognitive Processing in the Human Brain: Single Neuron Recordings in Depth-electrode Candidates for Epilepsy Surgery

Exploring the Neural Basis of Cognitive Processing in the Human Brain: Single Neuron Recordings in Depth-electrode Candidates for Epilepsy Surgery - Single Neuron Recordings in Depth-electrode Candidates

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON54764
Enrollment
50
Registered
2016-04-07
Start date
2016-06-10
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

epilepsy seizures

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Epilepsy patients with macro-electrode and micro-wire implants 18 years or older patients able to perform the experiments at an adequate level patients need to be mentally competent

Exclusion criteria

Exclusion criteria: IQ

Design outcomes

Primary

MeasureTime frame
The main study parameters are the macro- and microelectrode recordings of different brain areas during the performance of simple behavioural tasks and during stimulation of macro-electrode contacts. An important goal is to relate performance on the tasks to the neural data.

Secondary

MeasureTime frame
The secondary study parameters are the single- and multi-unit recordings and LFP during stimulation of the macro-contacts (if this is performed as part of the clinical assessment) and a functional MRI scan if an electrode is located in a visual area. We will also use data from two self/report questionnaires which will be administered both pre- and post-implantation. We will use the Beck Anxiety Inventory to assess anxiety and the Beck Depressivity Index to assess depression after the operation. These scores can be used to as co-regressors in our neural analyses. We will administer the questionnaire 3-4 days post-operatively to assess the patient*s state during the experimental phase at which we record the majority of our data.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)