OCD Clinical Trial
NCT number | NCT00399022 |
Other study ID # | SHEBA-06-4360-JZ-CTIL |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | November 13, 2006 |
Last updated | January 28, 2008 |
Testing the efficacy of the SNRI medication Duloxetine for treating OCD patients who did not respond to SSRI
Status | Withdrawn |
Enrollment | 40 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - OCD as main diagnosis according to DSM-IV - 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 treated with Duloxetine, currently or in the past - 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 |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Israel | Chaim Sheba Medical Center | Ramat-Gan |
Lead Sponsor | Collaborator |
---|---|
Sheba Medical Center |
Israel,
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