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Studies how brain stimulation affects memory in people with memory disorders

Tests intracranial brain stimulation in adults with epilepsy, memory problems or brain injury.

Plain-language title generated from the registry record
Registry title: Amygdala Memory Enhancement

Key facts

Where
St Louis, 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 75 years old?

Source: NCT05065450, who can take part

Where in United States

  • Washington University School of MedicineSt Louis, United StatesTaking people

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?
Print a page for my doctor

Trial details

Who runs it
Washington University School of Medicine
Trial code
NCT05065450
Record updated
17 July 2025
Original description
The objective is to understand how amygdala activation affects other medial temporal lobe structures to prioritize long-term memories. The project is relevant to disorders of memory and to disorders involving affect and memory, including traumatic brain injury and post-traumatic stress disorder.Read full original descriptionShow less

Mechanisms of Amygdala-Mediated Memory Enhancement in Humans

The objective is to understand how amygdala activation affects other medial temporal lobe structures to prioritize long-term memories. The project is relevant to disorders of memory and to disorders involving affect and memory, including traumatic brain injury and post-traumatic stress disorder.

Inclusion: Must be able to understand and speak English; Able to provide informed consent; Diagnosed with epilepsy; Scheduled to undergo long-term intra-cranial video monitoring for seizure onset localization; Must be implanted with intracranial depth electrodes to the left or right amygdala, hippocampus, and parahippocampal/perirhinal cortices.

Exclusion: Not diagnosed with epilepsy; Unable to understand and speak English; Unable to provide informed consent.

ClinicalTrials.gov NCT05065450