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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00792038
Other study ID # M-20080161
Secondary ID
Status Completed
Phase N/A
First received November 14, 2008
Last updated August 1, 2012
Start date January 2009
Est. completion date July 2012

Study information

Verified date August 2012
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection Agency
Study type Observational

Clinical Trial Summary

OCD patients are assessed before and after treatment using diagnostic tools, rating scales neuropsychological assessment and functional and structural MR-scans.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date July 2012
Est. primary completion date July 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. Steady state medication 3 months prior to the study

Exclusion Criteria:

1. History of head trauma or other organic brain disease

2. Pregnancy.

3. Pacemaker or other ferromagnetic materials in the body.

4. Comorbid psychiatric illnesses assessed using SCAN- interview (30) other than moderate depression (Ham-D<17) or anxiety disorders.

5. Antipsychotics

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Aarhus University Hospital, Risskov Risskov

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Y-Bocs Before and after treatment approx 20 weeks apart No
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