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Quantitative Electroencephalography (QEEG) and Low-resolution Electromagnetic Tomography (LORETA) Analysis in Post Traumatic Stress Disorder (PTSD) Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01020695
First Posted: November 25, 2009
Last Update Posted: November 7, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Doron Todder, Beersheva Mental Health Center
  Purpose
In this study the Quantitative Electroencephalography and low resolution topographic analysis of chronic Post-traumatic stress disorder and normal subjects will be compared.

Condition
Post-Traumatic Stress Disorder

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Retrospective
Official Title: QEEG and LORETA Analysis in PTSD Patients

Resource links provided by NLM:


Further study details as provided by Doron Todder, Beersheva Mental Health Center:

Enrollment: 10
Study Start Date: November 2009
Study Completion Date: November 2009
Primary Completion Date: November 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
PTSD veterans
18 PTSD veterans
controls
20 controls

  Show Detailed Description

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Veterans with chronic PTSD of at least 2 years.
Criteria

Inclusion Criteria:

  • 10 veterans suffering for PTSD according to the DSM-IV-TR for at least 2 years.
  • The 10 age matching controls will be recruited from the Beer Sheva mental stuff.

Exclusion Criteria:

  • Without any neurological or head trauma.
  • Without alcohol or substance abuse.
  • No evidence of psychotic episode in there history.
  • Stable doses of different specific serotonin reuptake inhibitors (SSRI) antidepressant for at least two months.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01020695


Locations
Israel
Beer Sheva Mental Health Center
Beer Sheva, Israel
Sponsors and Collaborators
Beersheva Mental Health Center
  More Information

Responsible Party: Doron Todder, Dr., Beersheva Mental Health Center
ClinicalTrials.gov Identifier: NCT01020695     History of Changes
Other Study ID Numbers: BHC-4917
First Submitted: November 23, 2009
First Posted: November 25, 2009
Last Update Posted: November 7, 2012
Last Verified: November 2012

Keywords provided by Doron Todder, Beersheva Mental Health Center:
PTSD
EEG
QEEG
LORETA

Additional relevant MeSH terms:
Stress Disorders, Traumatic
Stress Disorders, Post-Traumatic
Trauma and Stressor Related Disorders
Mental Disorders