Evaluation of Deep Transcranial Magnetic Stimulation (TMS) H-Coil in the Treatment of Major Depression

This study has been completed.
Sponsor:
Collaborator:
Brainsway
Information provided by:
Shalvata Mental Health Center
ClinicalTrials.gov Identifier:
NCT00445237
First received: March 7, 2007
Last updated: February 4, 2009
Last verified: March 2007

March 7, 2007
February 4, 2009
May 2006
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Complete list of historical versions of study NCT00445237 on ClinicalTrials.gov Archive Site
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Evaluation of Deep Transcranial Magnetic Stimulation (TMS) H-Coil in the Treatment of Major Depression
Evaluation of the H1 Coil and H2 Coil TMS Device - Safety and Feasibility in Major Depression Episode

This study is evaluating the safety and feasibility of the novel deep TMS H-coil designs in the treatment of resistant major depression in an open study using two different H-coil designs.

Not Provided
Interventional
Phase 1
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Major Depression
Device: H1 and H2 deep TMS coils
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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March 2008
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Inclusion Criteria:

  • Patients diagnosed as suffering from treatment resistant major depression

Exclusion Criteria:

  • Other axis I diagnosis
  • Risk factors for convulsions
  • Electroconvulsive therapy (ECT) in the last 9 months
  • History of drug abuse in the past year
Both
18 Years to 65 Years
No
Contact information is only displayed when the study is recruiting subjects
Israel
 
NCT00445237
SH-505
No
Not Provided
Shalvata Mental Health Center
Brainsway
Principal Investigator: Hilik Levkovits Day care hospital director
Shalvata Mental Health Center
March 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP