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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
  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

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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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
Anxiety Disorders
Mental Disorders
Stress Disorders, Traumatic

ClinicalTrials.gov processed this record on November 20, 2014