NCT00496925

Completed

Examining the Usage of Dopamine Blockers in OCD Patients

Sheba Medical Center Source

Other study identifiers

Sponsor study identifier

SHEBA- 07-4651-JZ-CTIL

Study Type

observational

Actual enrollment (reported)

63

Locations

1 country

Sites

1

Timeline

Study Start

November 2007

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

July 2009

Actual (reported)

Study Completion

July 2009

Actual (reported)

Brief 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.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 63 participants
Study completion date: July 2009
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
July 4, 2007
Actual (reported)
First Posted
July 6, 2007
Actual (reported)
Study Start
November 2007
Date type not reported
This date has not been verified as actual or estimated.
Primary Completion
July 2009
Actual (reported)
Study Completion
July 2009
Actual (reported)

Last Updated: February 2, 2010
Status Verified: January 2010
Last Update Submitted: January 31, 2010

Conditions

Obsessive Compulsive Disorder

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodProbability Sample

Study Population

Outpatient and Inpatients

You may qualify if:

Patients over 18 years of age
DSM-IV diagnosis of OCD
Ability to understand patient information sheet, and consent to participate

You may not qualify if:

Current or past Psychotic or Bipolar disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Sheba Medical Center
Governmentlead

Study Sites (1)

Chaim Sheba Medical Center

Ramat Gan, 52621, Israel

MeSH Terms

Conditions

Obsessive-Compulsive Disorder

Condition Hierarchy (Ancestors)

Anxiety DisordersMental Disorders

Study Officials

Joseph Zohar, MD
Chaim Sheba Medical Center
PRINCIPAL INVESTIGATOR

Enrollment

63 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: CROSS SECTIONAL
Sponsor Type: OTHER GOV

Study Record Dates

First Submitted

July 4, 2007

First Posted

July 6, 2007

Study Start

November 2007

Date type not reported

This date has not been verified as actual or estimated.

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Primary Completion

July 2009

Actual (reported)

Study Completion

July 2009

Actual (reported)

Last Updated

February 2, 2010

Record last verified: 2010-01

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00496925
Data provider: ClinicalTrials.gov
Source updated: 2010-02-02
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:34:08 UTC

Locations

IL(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

First Submitted

First Posted

Study Start

Primary Completion

Study Completion

Conditions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations