Neuronetics, a firm based in Malvern, Pennsylvania, won FDA approval for its latest NeuroStar transcranial magnetic stimulation therapy system. Approved in the U.S. for treating depression in patients who have tried at least one antidepressant drug, the new system has the major benefit of offering the same therapy during shorter sessions. Although session duration is decided on by the physician, many sessions can be complete within twenty minutes.

This technology is not to be confused with electroconvulsive therapy that sends electric current through the brain, instead relying on focused magnetic fields that don’t seem to cause any serious side effects.

The system features laser positioning and a sensor that feels the contact pressure of the magnetic field generator against the head, helping to get therapy sessions started quickly and with little discomfort.

Discover The World's MOST COMPREHENSIVE Mental Health Assessment Platform

Efficiently assess your patients for 80+ possible conditions with a single dynamic, intuitive mental health assessment. As low as $12 per patient per year.

Some details from Neuronetics:

The majority of people who benefited from treatment with NeuroStar experienced clinically meaningful, long-lasting improvement; NeuroStar had proven durability over 12 months in an open-label clinical trial. Additionally, over the past year, there has been approximately a 20 percent increase in the number of NeuroStar systems across the country — further increasing patient access to this transformative treatment.

NeuroStar is indicated for the treatment of MDD in adult patients who have failed to receive satisfactory improvement from prior antidepressant medication in the current episode. In an NIMH-funded, independent, randomized controlled trial, patients treated with TMS using a clinical-trial version of the NeuroStar TMS System were four times more likely to achieve remission compared to patients receiving sham treatment (P = 0.0173; odds ratio = 4.05).

The most common side effect is pain or discomfort at or near the treatment site, which usually resolves within one week. It is contraindicated in people with non-removable conductive metal in or near the head. Long term durability of effect has not been established in a randomized controlled trial.

Hot daily news right into your inbox.