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Transcranial Magnetic Stimulation in Depression
This study has been completed.
Study NCT00018746   Information provided by Department of Veterans Affairs
First Received: July 3, 2001   Last Updated: January 20, 2009   History of Changes

July 3, 2001
January 20, 2009
July 1999
 
 
 
Complete list of historical versions of study NCT00018746 on ClinicalTrials.gov Archive Site
 
 
 
Transcranial Magnetic Stimulation in Depression
Efficacy of Threshold vs. Subthreshold TMS in the Treatment of Depression

The study examines efficacy of repetitive transcranial magnetic stimulation in treating severely depressed patients who are medicated.

Medicated, treatment resistant, depressed patients are randomized to active or sham repetitive transcranial magnetic stimulation (rTMS). Responding patients go into a six months follow-up period.

Phase I
Interventional
Treatment, Randomized, Single Blind, Placebo Control, Crossover Assignment, Efficacy Study
Depression
Device: repetitive transcranial magnetic stimulation
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
July 2001
 

severe treatment-resistant depression

Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00018746
 
MHBS-037-98S
Department of Veterans Affairs
 
Investigator: Ralph Hoffman
Investigator: Dan Oren
Department of Veterans Affairs
December 2004

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