Ensayos clínicos

Inclusion Criteria:

• Provision of signed and dated informed consent form.
• Stated willingness to comply with all study procedures and availability for the duration of the study.
• Male or female, 18 years of age or older.
• In good general health as evidenced by medical history but may include a diagnosis of epilepsy.
• Volunteers who are confirmed to have temporal lobe epilepsy based on established medical history and have established outpatient epilepsy care within the Mayo Clinic Health System.

Exclusion Criteria:

• Participants with a contraindication to MRI. Such contraindications include, but are not limited to: pacemaker, metallic cardiac valve(s), magnetic material such as surgical clips, tattoos, implanted electronic infusion pumps or any other condition that would interfere with the MRI, a stent somewhere in the body, a history of allergic reaction to any metals.
• Participants who have structural anatomical legions outside the medial temporal lobe.
• Pregnancy or lactation.
• Participants who report previous experience with claustrophobia, anxiety and/or vertigo when moved inside the scanner.
• Febrile illness within the last thirty days.
• Treatment with another investigational drug or other intervention within the last thirty days.
• Subjects incapable of giving informed written consent.
•  Participants in the prisoner population.

Eligibility last updated 8/26/21. Questions regarding updates should be directed to the study team contact.