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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00496925
Other study ID # SHEBA- 07-4651-JZ-CTIL
Secondary ID
Status Completed
Phase N/A
First received July 4, 2007
Last updated January 31, 2010
Start date November 2007
Est. completion date July 2009

Study information

Verified date January 2010
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

We examine the usage of Dopamine blockers in OCD patients. We want to examine their frequency of usage, compare the course of the disease between those who receive and those who do not receive Dopamine blockers, and efficacy of the treatment.

The study will be done in two stages: 1. Collecting information the usage of Dopamine blockers from 150 OCD patients' files. 2. interviewing 60-70 patients to see the difference those who receive and those who do not receive Dopamine blockers in their current severity of disease.


Recruitment information / eligibility

Status Completed
Enrollment 63
Est. completion date July 2009
Est. primary completion date July 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients over 18 years of age

- DSM-IV diagnosis of OCD

- Ability to understand patient information sheet, and consent to participate

Exclusion Criteria:

- Current or past Psychotic or Bipolar disorder

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


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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