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Acetylcysteine Augmentation in Treatment of Refractory Obsessive-Compulsive Disorder

Phase 2
Conditions
Obsessive-compulsive disorder.
Obsessive-compulsive disorder
Registration Number
IRCT201103243930N4
Lead Sponsor
Vice chancellor for research, Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Inclusion Criteria are: DSM-IV diagnosis of OCD; symptoms of at least 1 year duration, moderate to severe OCD symptoms (Y-BOCS > 16), and failure of an adequate trial of an SSRI.
Exclusion Criteria are: primary diagnosis of a psychotic disorder, active substance abuse or dependence, unstable medical condition, prior exposure to N-Acetylcysteine, pregnancy, breastfeeding, or intent to become pregnant during study, evidence of active liver disease, seizure disorder, and active suicidal ideation.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Yale-Brown Obsessive-Compulsive Scale. Timepoint: every 2 weeks for 10 weeks. Method of measurement: Interview.
Secondary Outcome Measures
NameTimeMethod
Clinical Global Impression. Timepoint: every 2 weeks for 10 weeks. Method of measurement: Self-report.
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