Breakthrough PTSD treatment achieves 68% remission rate in clinical trial

A new PTSD treatment utilizing brain activity measurements to guide targeted magnetic stimulation has received FDA clearance. Clinical trials reported a 68% remission rate, significantly outperforming traditional medication and psychotherapy outcomes.
Why it matters
This technology offers a promising, personalized alternative for the millions of people, including veterans, who do not find relief through standard PTSD treatments.
A new approach to treating post-traumatic stress disorder (PTSD) has received FDA clearance, offering a personalized alternative for people who have not found sufficient relief through existing treatments. Developed by California-based Wave Neuroscience in collaboration with researchers at the Texas A&M Health Institute of Biosciences and Technology, the technology uses brain activity measurements to guide targeted magnetic stimulation.
Early clinical trial findings have been encouraging. According to Wave Neuroscience, patients experienced a 52% reduction in PTSD symptoms, while 68% achieved remission. The full findings are still being prepared for public release, but researchers believe the technology could significantly expand treatment options for millions of people.
The need for more effective PTSD care is substantial. In the United States, approximately 17.5 veterans die by suicide each day , and about 7% of veterans receive a PTSD diagnosis annually.
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