107 0 Kommentare NeuroStar Advanced Therapy Outcomes Registry Clinical Data Published in Brain Stimulation Validates Depression Treatment Protocols - Seite 2

The results showed:

Strong efficacy obtained with the shorter ITIs allows clinicians to efficiently treat a larger number of patients
The Standard and Dash protocols did not differ in number of treatment sessions, and both manifested strong antidepressant effects
Response rates were notably as high as 72 percent among study samples
Remission rates were notably as high as 53 percent among study samples

“The NeuroStar Outcomes Registry data continues to support the safety and efficacy of our treatment protocols for patients who haven’t had success with antidepressant medications, and we’re excited to have the research published and shared with the broader clinical community,” said Keith J. Sullivan, President and CEO of Neuronetics. “The shortened Dash protocol not only means clinicians are able to treat more patients in need, but also that patients have access to an effective, more convenient treatment option. I’m grateful to the NeuroStar providers who contribute to the Outcomes Registry; it is research like this that informs treatment progress and advancements.”

The research published in Brain Stimulation follows the publication of registry data in the Journal of Affective Disorders in December 2020, which suggested NeuroStar Advanced Therapy be studied and evaluated as a first-line treatment for Major Depressive Disorder.

The NeuroStar Advanced Therapy system can be offered in three treatment variations in order to expand access and availability: Standard, which offers treatments at 38 minutes per session; Dash, which offers treatments as little as 19 minutes per session; and TouchStar theta burst, which offers treatments at three minutes per session. Visit www.neurostar.com for more information.

About Neuronetics
Neuronetics, Inc. is a commercial-stage medical technology company focused on designing, developing, and marketing products that improve the quality of life for patients who suffer from psychiatric disorders. Its commercial product, the NeuroStar Advanced Therapy System, is a non-invasive and non-systemic office-based treatment that uses transcranial magnetic stimulation, or TMS, to create a pulsed, MRI-strength magnetic field that induces electrical currents designed to stimulate specific areas of the brain associated with mood. The system is cleared by the United States Food and Drug Administration, or FDA, for the treatment of major depressive disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. Visit NeuroStar.com for safety information and indications for use. NeuroStar is also available in other parts of the world, including Japan, where it is listed under Japan’s national health insurance. Additional information can be found at https://neurostar.com/neuronetics/.