Obsessive-compulsive Disorder Clinical Trial
Official title:
Topiramate Augmentation in the Treatment of Obsessive-Compulsive Disorder
NCT number | NCT00211744 |
Other study ID # | 04-0379 |
Secondary ID | |
Status | Completed |
Phase | Phase 4 |
First received | |
Last updated | |
Start date | August 2004 |
Est. completion date | August 2006 |
Verified date | May 2018 |
Source | Montefiore Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A 12-week program to examine the effectiveness of topiramate in adjunctive treatment for adults with obsessive-compulsive disorder and who are currently on serotonin reuptake inhibitor medications (ages 18-65).
Status | Completed |
Enrollment | 24 |
Est. completion date | August 2006 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: Males and Females 18-65 years of age diagnosed with OCD and currently taking SSRI medication(s) Exclusion Criteria: major medical disorders |
Country | Name | City | State |
---|---|---|---|
United States | Mount Sinai School of Medicine | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Montefiore Medical Center | Ortho-McNeil Pharmaceutical |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To evaluate the safety and efficacy of adjunctive topiramate vs. placebo in the treatment of OCD |
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