Status:

WITHDRAWN

rTMS for Treatment of Depressed Phase of Bipolar Disorder Type II

Lead Sponsor:

University of Texas Southwestern Medical Center

Collaborating Sponsors:

Stanley Medical Research Institute

Neuronetics

Conditions:

Bipolar Disorder

Eligibility:

All Genders

18-65 years

Phase:

PHASE2

Brief Summary

This research study evaluates an experimental device for the treatment of the depressed phase of Bipolar Disorder Type II. Repetitive Transcranial Magnetic Stimulation (rTMS) is an experimental proced...

Detailed Description

This is a double-blind randomized controlled trial of rTMS for outpatients in the depressive phase of BD-II. Participants will be evaluated at UT Southwestern Medical Center at Dallas. Forty eligible ...

Eligibility Criteria

Inclusion

  • Male and female outpatients aged 18-55 years old
  • Meet DSM-IV criteria for Bipolar Affective Disorder Type II, depressed phase without psychosis as determined by Structured Clinical Interview for DSM-IV
  • A MADRS ≥ 15 at Initial Visit, and at Prior to TMS Evaluation
  • A Young Mania Rating Scale \< 12 at Initial Visit and at Prior to TMS Evaluation
  • Duration of current episode of depression \>2 months but ≤ 1 year of unsuccessful treatment
  • On stable medication and/or psychotherapy for 1 month and clinically appropriate to maintain for duration of trial
  • Cognitively intact (Folstein MMSE score \>24).
  • Clinically competent to give informed written consent

Exclusion

  • History of epilepsy or seizure disorder, mass brain lesions, cerebrovascular accident, metal in the skull, a history of major head trauma, or any neurologic condition likely to increase risk of rTMS.
  • Suicidal risk that precludes safe participation defined as score of 5 or 6 on MADRS item 10 Suicidal Thoughts or clinical impression that the subject is at significant risk for suicide.
  • History of any DSM-IV Axis I diagnosis other than Bipolar Affective Disorder Type II, depressed phase, simple phobia and generalized anxiety disorder (GAD) in the last year
  • Lifetime history of schizophrenia, schizoaffective, or other psychotic disorder, bipolar disorder type I, dementia, dissociative disorders, and sexual and gender identity disorder
  • Personality disorder that makes participation in the trial difficult
  • Greater than or equal to 8 episodes of mood disturbance in the previous 12 months
  • Greater than 4 unsuccessful treatments in current episode
  • History of Substance Abuse or Dependence (DSM-IV) in the last year except nicotine and caffeine
  • Positive urine drug test during screening
  • Taking any medication that significantly lowers the seizure threshold (e.g. lithium, stimulants, bupropion, TCAs, antipsychotics, theophylline, etc.)
  • Unstable medical conditions that precludes safe participation in rTMS treatment trial
  • Known or suspected pregnancy
  • Women of child-bearing potential not using medically accepted form of contraception when engaged in sexual intercourse
  • Any metal or device implants that would increase risk of rTMS
  • Unable to determine the motor threshold in the subject
  • History of Vagus Nerve Stimulation
  • Currently in another investigational study
  • Prior electroconvulsive therapy failure

Key Trial Info

Start Date :

February 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2010

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT00447096

Start Date

February 1 2007

End Date

February 1 2010

Last Update

June 9 2016

Active Locations (1)

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1

UT Southwestern Medical Center at Dallas

Dallas, Texas, United States, 75390