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Augmentation therapy comparison in refractory obsessive-compulsive disorder with Aripiprazole vs. Risperidone

Not Applicable
Conditions
Obsessive-compulsive disorder.
Obsessive-compulsive disorder
Registration Number
IRCT2015110424882N1
Lead Sponsor
Kashan University of Medical Sciences, Dr Gholamali Hamidi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Age between 18-60 years;the Yale-Brown obsessive-compulsive scale (Y-BOCS) =16 and suffering from OCD whilst were taken a therapeutic dose of SSRI drugs at least for 12 weeks;negative history of: pregnant or breastfeeding in women; psychotic, bipolar mood, and severe depressive disorders in DSM-IV-TR axis I; any known disorder in DSM-IV-TR axis II like personality disorders or mental retardation; drug and alcohol abuse in the last six months before study; any physical disease impeding the use of Risperidone or Aripiprazole; not psychotherapy during the study.
Exclusion criteria: Any acute or severe physical diseases occurring during the study; more than four weeks loss to follow-up; severe side effects during the study; not using contraceptive methods in females.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of symptoms of OCD. Timepoint: Basline and every 4 weeks. Method of measurement: Y_BOCS.
Secondary Outcome Measures
NameTimeMethod
nwanted side effects of drugs. Timepoint: Every 4 weeks. Method of measurement: Interview.
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