Stress Disorders, Post-Traumatic Clinical Trial
Official title:
Electroencephalogram (EEG) Personalized Transcranial Magnetic Stimulation (eTMS) for Post-Traumatic Stress Disorder
Verified date | May 2024 |
Source | Wave Neuroscience |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is an open-label safety pilot study of the Electroencephalogram (EEG) Transcranial Magnetic Stimulation (eTMS) treatment for Post-Traumatic Stress Disorder (PTSD). The recruitment goal is 30 participants who are United States Military veterans or first responders (e.g., firefighters, police, paramedics, etc.). The Study includes an EEG recording in order to determine the optimal treatment parameters for the eTMS system, followed by 10 in-office visits that take place over 21 total days. Two eTMS treatment sessions are administered during each office visit.
Status | Completed |
Enrollment | 30 |
Est. completion date | May 16, 2024 |
Est. primary completion date | May 16, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 22 Years to 65 Years |
Eligibility | Inclusion Criteria: - Willing and able to consent to participate in the study via signed Informed Consent - Age 22 - 65 years - Provisional diagnosis of PTSD - Positive identification as either a Veteran, or First Responder (e.g., emergency medical service provider, firefighter, or any other emergency response personnel) Exclusion Criteria: - Uncontrolled medical, psychological or neurological condition - Pregnant, or female unwilling to use effective birth control during the course of the trial - Metal objects implanted in the head - Past exposure to metal fragments or other metal sources in the head and neck - Current participation in any interventional research protocol - History of any type of Electroconvulsive Therapy (ECT) or TMS - History of stroke or intracranial lesion, or increased intracranial pressure - History or epilepsy or seizure - Family history of epilepsy or seizure in 1st degree relative. |
Country | Name | City | State |
---|---|---|---|
United States | Wright State University | Dayton | Ohio |
Lead Sponsor | Collaborator |
---|---|
Wave Neuroscience |
United States,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Treatment Safety | Incidence, severity, relatedness, type, subsequent treatment/intervention required, and resolution status of adverse events during the study | Assessed at all treatment sessions and Follow-up Visit, a duration of up to 5 weeks |
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