Status:

COMPLETED

Treating Refractory Obsessive Compulsive Disorder With rTMS

Lead Sponsor:

Centre for Addiction and Mental Health

Conditions:

Obsessive Compulsive Disorder

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

Obsessive-compulsive disorder (OCD) is a severe psychiatric condition with only limited response to current first-line treatments, comprising pharmacotherapy and cognitive-behavioural therapy. Repetit...

Detailed Description

Obsessive-compulsive disorder (OCD) is a severe and debilitating psychiatric illness characterized by intrusive unwanted thoughts (obsessions) and repetitive or ritualistic actions intended to reduce ...

Eligibility Criteria

Inclusion

  • voluntary and competent to consent based on their ability to provide a spontaneous narrative description of the key elements of the study
  • have a Structured Clinical Interview for DSM-IV (SCID) confirmed diagnosis of OCD
  • are between the ages of 18 and 65
  • have failed to achieve a clinical response, or did not tolerate, at least 3 separate antidepressant trials of sufficient dose for at least 10 weeks
  • have a score of greater than or equal to 17 on the Y-BOCS. A careful medical and neurological history will be taken to ensure that subjects have no unstable conditions that would preclude them from entering into the study. This history will focus on conditions such as seizures, stroke, hypertension, diabetes, coronary artery disease, thyroid problems, respiratory illness, allergies and presence of metal implants

Exclusion

  • have a history of DSM-IV substance dependence in the last 6 months, and have DSM-IV substance abuse in the last month
  • have a concomitant major unstable medical or neurologic illness or have had a history of seizures
  • acutely suicidal
  • are pregnant
  • have metal implants. With respect to concomitant medications, patients will be excluded if they are currently (or in the last 4 weeks) taking: (a) more than lorazepam 2 mg daily (or equivalent), (b) monoamine oxidase inhibitors, (c) and/or bupropion due to its associated increased risk for seizures.

Key Trial Info

Start Date :

June 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2011

Estimated Enrollment :

19 Patients enrolled

Trial Details

Trial ID

NCT00396552

Start Date

June 1 2006

End Date

December 1 2011

Last Update

February 15 2013

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada, M4N 3M5

2

Centre for Addiction and Mental Health

Toronto, Ontario, Canada, M5T 1R8