Effects of Levetiracetam (Keppra) on Alcohol Consumption
NCT01168687 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46
Last updated 2020-08-28
Summary
The overall goals of this study are to (1) expand knowledge about interactions of levetiracetam with alcohol by assessing the effects of levetiracetam compared to placebo in moderate and heavy social alcohol users and (2) to test the AccuswayTM platform as a tool to measure postural control (which has been used as a marker of intoxication) and the effects of levetiracetam on postural control.
Conditions
- Alcohol Abuse
- Drug Abuse
Interventions
- DRUG
-
Levetiracetam (Keppra)
Group A: Twenty moderate to heavy social alcohol users will receive 250 mg of levetiracetam BID (500 mg/day) or placebo x 7 days and will be titrated to a maximum dose of 500 mg of levetiracetam BID (1,000 mg/day) x 7 days. Group B: Twenty moderate to heavy social alcohol users will receive 500 mg levetiracetam BID (1000 mg/day) or placebo x 7 days and will be titrated to a maximum dose of 1000 mg levetiracetam BID (2,000 mg per day) x 7 days.
- DRUG
Sponsors & Collaborators
-
United States Department of Defense
collaborator FED -
University of California
collaborator OTHER -
University of California, San Francisco
lead OTHER
Principal Investigators
-
Robert O. Messing, M.D. · UCSF; Department of Neurology; Ernest Gallo Clinic and Research Center
-
Jennifer M. Mitchell, Ph.D. · UCSF; Department of Neurology; Ernest Gallo Clinic and Research Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 21 Years
- Max Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-11-30
- Primary Completion
- 2009-11-30
- Completion
- 2010-11-30
Countries
- United States
Study Locations
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