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Sponsored by: |
Hadassah Medical Organization |
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Information provided by: | Hadassah Medical Organization |
ClinicalTrials.gov Identifier: | NCT00517400 |
Evaluation of the novel deep TMS H-Coil designs as a treatment measure in post traumatic stress disorder (PTSD).
Comparing real to sham treatment.
Condition | Intervention | Phase |
---|---|---|
Post Traumatic Stress Disorder |
Device: Deep repetitive Transcranial Magnetic Stimulation (rTMS) |
Phase I Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind (Subject), Parallel Assignment |
Official Title: | Evaluation of the H-Coil Transcranial Magnetic Stimulation (TMS) Device- Treatment for Post Traumatic Stress Disorder |
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Moshe Isserles, MD, MSc | 972-2-6779308 | dr.isserles@yahoo.com |
Contact: Abraham I Zangen, PhD | 972 8 9344415 |
Principal Investigator: | Moshe Isserles, MD, MSc | Hadassah Medical Organization |
Study ID Numbers: | 364/3.8.07(HMO) |
Study First Received: | August 16, 2007 |
Last Updated: | August 16, 2007 |
ClinicalTrials.gov Identifier: | NCT00517400 |
Health Authority: | Israel: Ministry of Health, Health Technology and Infrastructure Administration, Medical Device Department |
PTSD |
Anxiety Disorders Mental Disorders Stress Disorders, Post-Traumatic Stress Stress Disorders, Traumatic |
Pathologic Processes Disease |