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Treatment With Duloxetine for OCD Patients

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00399022
Enrollment
40
Registered
2006-11-14
Start date
Unknown
Completion date
Unknown
Last updated
2008-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

OCD

Brief summary

Testing the efficacy of the SNRI medication Duloxetine for treating OCD patients who did not respond to SSRI

Interventions

DRUGDuloxetine

Sponsors

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026