Status:

COMPLETED

rTMS Treatment in Patients With General Anxiety Disorder

Lead Sponsor:

Queen's University

Collaborating Sponsors:

Military Medical Academy, Bulgaria

Conditions:

Generalized Anxiety Disorder

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

This study will compare the change detected by a standardized rating scale (Hamilton Anxiety Rating Scale) scores in the active treatment group as compared to sham (placebo) group after 6 weeks of rTM...

Eligibility Criteria

Inclusion

  • signed patient informed consent;
  • primary GAD diagnosis;
  • HARS \>=15;
  • male/female 18-65 years;
  • without GAD pharmacotherapy at least last 2 weeks or if they are taking GAD medication it must be stable for at least 6 weeks prior to the start of the study and not be changed during the 6 weeks of the study treatment phase.
  • Individual or group supportive psychotherapy may continue during the study but will not be allowed to start new psychotherapy during the 6 weeks of the study treatment phase.

Exclusion

  • current serious Axis I schizophrenia, bipolar I, MDD;
  • other primary Axis I in the opinion of investigator;
  • HDRS \>=18;
  • metallic implant in cranium except mouth;
  • severe/unstable medical conditions;
  • ect within last 3 months;
  • history epilepsy;
  • neurological disorder leading to increased intracranial pressure;
  • severe cardiac disorder/intracardiac lines/pacemakers;
  • current suicide risk.

Key Trial Info

Start Date :

January 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2012

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT00616447

Start Date

January 1 2008

End Date

November 1 2012

Last Update

December 16 2015

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Military Medical Academy

Sofia, Bulgaria

2

Providence Care Mental Health Services

Kingston, Ontario, Canada, K7L4X3

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