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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00229372
Other study ID # SHEBA-02-2732-JZ-CTIL
Secondary ID
Status Completed
Phase N/A
First received September 28, 2005
Last updated January 28, 2008
Start date November 2006
Est. completion date April 2007

Study information

Verified date January 2008
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

Assessing the efficacy of Posttraumatic Stress Disorder (PE) treatment for chronic Posttraumatic Stress Disorder (PTSD)


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date April 2007
Est. primary completion date April 2007
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- PTSD

Exclusion Criteria:

- Psychotic symptoms

- Dissociation

- Drug or Alcohol dependence

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind


Intervention

Behavioral:
Prolonged Exposure (PE) therapy


Locations

Country Name City State
Israel Chaim Sheba Medical Center Ramat-Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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