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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00229320
Other study ID # SHEBA-05-3679-JZ-CTIL
Secondary ID
Status Completed
Phase N/A
First received September 28, 2005
Last updated January 28, 2008
Start date February 2005
Est. completion date November 2005

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 OCD before and after group therapy


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date November 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- OCD

- Eligibility to participate in group therapy

Exclusion Criteria:

- PTSD

- Suicidal thoughts

- Psychotic state

- Severe hostile personality disorder

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Intervention

Behavioral:
Group 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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