Trials / Completed
CompletedNCT00595699
Escitalopram Treatment of Major Depression in Patients With Temporal Lobe Epilepsy
Escitalopram Treatment of Major Depression in Patients With Temporal Lobe Epilepsy. A Double-blind, Placebo-controlled Study.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 8 (actual)
- Sponsor
- Conrad, Erich J., M.D. · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This is a research study evaluating the use of escitalopram (Lexapro®) for the treatment of major depression in subjects with temporal lobe epilepsy. The purpose of the study is to measure the severity and change in depressive and anxiety symptoms after 10 weeks of study treatment with escitalopram or placebo as measured by certain rating scales and questionnaires. In addition, the study will measure the frequency of seizures using a patient diary during the study. Finally, the study will assess the change in the quality of life using rating scales.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | escitalopram | 10 mg daily for the first week followed by an increase to 20 mg daily for the remainder of the study |
| DRUG | placebo | Placebo |
Timeline
- Start date
- 2006-11-01
- Primary completion
- 2009-12-01
- Completion
- 2009-12-01
- First posted
- 2008-01-16
- Last updated
- 2011-07-18
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00595699. Inclusion in this directory is not an endorsement.