Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
NA
40 participants
INTERVENTIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Interventions
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Duloxetine
Eligibility Criteria
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Inclusion Criteria
* Age 18 to 65
* Men and women
* YBOCS score is 18 or more, or 12 or more in case of only obsessions
Exclusion Criteria
* Patients having comorbid schizophrenia or psychotic disorder or bipolar disorder Patients with substance abuse disorder in the last 6 months Patients who were suicidal or did serious suicide attempt in the last year Pregnant or lactating women, or woman of childbearing potential, which is not using adequate contraception Patients with neurologic disturbance or disorder Patients with serious or imbalanced medical condition Patients with allergic response to SSRI or duloxetine Patients who started new treatment (CBT or pharmacology) in less than 3 months
18 Years
65 Years
ALL
No
Sponsors
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Sheba Medical Center
OTHER_GOV
Responsible Party
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Chaim Sheba Medical Center
Principal Investigators
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Joseph Zohar, MD
Role: PRINCIPAL_INVESTIGATOR
Chaim Sheba Medical Center
Locations
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Chaim Sheba Medical Center
Ramat Gan, , Israel
Countries
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Other Identifiers
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SHEBA-06-4360-JZ-CTIL
Identifier Type: -
Identifier Source: org_study_id