Assessment of Suicidality in Epilepsy - Rating Tools
NCT01085461 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2012-03-05
Summary
This will be a cross-sectional study enrolling 200 outpatients/inpatients with treatment resistant partial epilepsy for at least two years, receiving 1-3 AEDS.
The study will consist of one or two visits, each lasting 1-2 hours. All subjects will complete Visit 1. Twenty five percent of the subjects will return for Visit 2. The study will assess the prevalence of depression and suicidal thoughts and the feasibility of using the proposed psychiatric rating scales in future epilepsy clinical trials. This study will also provide an estimate of the proportion of patients with epilepsy (PWE) who may be ineligible for future trials.
Conditions
Sponsors & Collaborators
-
Eisai Inc.
collaborator INDUSTRY - collaborator INDUSTRY
-
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
collaborator INDUSTRY -
H. Lundbeck A/S
collaborator INDUSTRY - collaborator INDUSTRY
-
Supernus Pharmaceuticals, Inc.
collaborator INDUSTRY -
UCB Pharma
collaborator INDUSTRY -
Upsher-Smith Laboratories
collaborator INDUSTRY -
The Epilepsy Study Consortium
lead OTHER
Principal Investigators
-
Jacqueline French, M.D. · NYU Langone Medical Center
-
Andres Kanner, M.D. · Rush University Medical Center
-
Dale Hesdorffer, PhD, MPH · Columbia University
-
Kelly Posner, PhD · Columbia University
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-01-31
- Completion
- 2011-12-31
Countries
- United States
Study Locations
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