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Studies brain thalamus areas in people with epilepsy and memory

Studies how brain thalamus regions connect and affect seizures and memory in adults with epilepsy.

Plain-language title generated from the registry record
Registry title: Human Thalamus in Propagation of Temporal Lobe Seizures and Memory Formation

Key facts

Where
Stanford, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07226908, who can take part

Where in United States

  • Stanford HospitalStanford, United StatesNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Stanford University
Trial code
NCT07226908
Record updated
12 November 2025
Original description
The goal of the study is to examine how two key subregions of the human thalamus (ANT and PLV) are connected with other brain structures (Aim 1), how seizures involve the two thalamic subregions differently and how the map of cortico-thalamic ictal propagation matches the intrinsic connectivity maps identified in the same individuals (Aim 2), and the effect of ANT and PLV stimulations on memory formation (Aim 3).Read full original descriptionShow less

Human Thalamus in Propagation of Temporal Lobe Seizures and Memory Formation

The goal of the study is to examine how two key subregions of the human thalamus (ANT and PLV) are connected with other brain structures (Aim 1), how seizures involve the two thalamic subregions differently and how the map of cortico-thalamic ictal propagation matches the intrinsic connectivity maps identified in the same individuals (Aim 2), and the effect of ANT and PLV stimulations on memory formation (Aim 3).

Inclusion: No medical or surgical contraindication to electrode implantation; Patient capable of understanding the scope of our project or signing informed consent independently.

Exclusion: Unable to provide informed consent.

ClinicalTrials.gov NCT07226908