NeuroStar TMS Therapy® — Proven Efficacy

Clinical Results: Randomized Controlled Trial1

Primary diagnosis:  DSM-IV Major Depressive Disorder

Antidepressant Treatment History (Indicated Population)

NeuroStar Randomized Controlled Trial Key Outcome Measure (Indicated Population) – Change Score in Montgomery Asberg Depression Rating Scale (MADRS)

Change Score in Montgomery Asberg Depression Rating Scale (MADRS)

In this controlled clinical trial, patients received an average reduction in their depression symptom score of 22.1% with active NeuroStar TMS Therapy as compared to a 9% average reduction in patients receiving inactive (sham) treatment.  Statistical significance in favor of active NeuroStar TMS was observed as early as 2 weeks after treatment and at 4 and 6 weeks.

Treatment Utilization and Outcomes Study2

Patient Population & Sites

Study Duration

NeuroStar Outcomes Data

The results of the open-label Outcomes study are consistent with prior open-label outcomes for NeuroStar TMS Therapy, in which 1 in 2 patients suffering with depression improved significantly, and 1 in 3 patients were completely free of depression symptoms after six weeks of treatment.3

View NeuroStar TMS Therapy Safety Data

 

  1. O’Reardon, J. P., H. B. Solvason, et al. (2007). “Efficacy and Safety of Transcranial Magnetic Stimulation in the Acute Treatment of Major Depression:  A Multisite Randomized Controlled Trial.” Biol Psychiatry 62(11): 1208-1216.
  2. Neuronetics, Inc. (data on file, 2012)
  3. Demitrack MA, Thase ME. Clinical significance of transcranial magnetic stimulation (TMS) in the treatment of pharmacoresistant depression: synthesis of recent data. Psychopharm Bull. 2009, 42(2): 5-38.