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Characteristics of Post-Traumatic Stress Disorder (PTSD) and Non-PTSD Subjects

This study has been completed.
Sponsor:
Information provided by:
Sheba Medical Center
ClinicalTrials.gov Identifier:
NCT00229359
First received: September 28, 2005
Last updated: December 18, 2007
Last verified: December 2007
History of Changes
  Purpose

Compare PTSD and non-PTSD subjects on several demographic, cognitive and military variables


Condition
PTSD

Study Type: Observational
Official Title: Risk Factors for PTSD

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Sheba Medical Center:

Study Start Date: January 2000
Estimated Study Completion Date: December 2002
  Eligibility

Criteria

Inclusion Criteria:

  • Subjects applied for treatment in the MOH rehabilitation centers or the IDF unit for combat reactions and were diagnosed with PTSD

Exclusion Criteria:

-

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00229359

Sponsors and Collaborators
Sheba Medical Center
Investigators
Principal Investigator: Joseph Zohar, MD Tel Aviv University
  More Information

No publications provided by Sheba Medical Center

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

ClinicalTrials.gov Identifier: NCT00229359     History of Changes
Other Study ID Numbers: SHEBA-99-1813-JZ-CTIL
Study First Received: September 28, 2005
Last Updated: December 18, 2007
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Additional relevant MeSH terms:
Stress Disorders, Post-Traumatic
Stress Disorders, Traumatic
Anxiety Disorders
Mental Disorders

ClinicalTrials.gov processed this record on May 19, 2013