A Double-Blind, Placebo-Controlled Trial Assessing the Efficacy of Levetiracetam Extended-Release in Very Heavy Drinking Alcohol-Dependent Patients

被引:44
作者
Fertig, Joanne B. [1 ]
Ryan, Megan L. [1 ]
Falk, Daniel E. [1 ]
Litten, Raye Z. [1 ]
Mattson, Margaret E. [2 ]
Ransom, Janet [3 ]
Rickman, William J. [3 ]
Scott, Charles [3 ]
Ciraulo, Domenic [4 ]
Green, Alan I. [5 ]
Tiouririne, Nassima A. [6 ]
Johnson, Bankole [7 ]
Pettinati, Helen [8 ]
Strain, Eric C. [9 ]
Devine, Eric [4 ]
Brunette, Mary F. [10 ]
Kampman, Kyle [8 ]
Tompkins, David A. [9 ]
Stout, Robert [11 ]
机构
[1] NIAAA, Div Treatment & Recovery Res, Bethesda, MD USA
[2] Subst Abuse & Mental Hlth Serv Adm SAMHSA, Ctr Behav Hlth Stat & Qual, Rockville, MD USA
[3] FastTrack Drugs & Biol, N Potomac, MD USA
[4] Boston Univ, Sch Med, Boston, MA 02118 USA
[5] Dartmouth Med Sch DHMC, Dept Psychiat, Lebanon, NH USA
[6] Univ Virginia, Ctr Addict Res & Educ, Richmond, VA USA
[7] Univ Virginia, Dept Psychiat Med, Ctr Addict Res & Educ, Charlottesville, VA USA
[8] Univ Penn, Treatment Res Ctr, Perelman Sch Med, Philadelphia, PA 19104 USA
[9] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21205 USA
[10] Dartmouth Med Sch, Dept Psychiat, Psychopharmacol Res Grp, Concord, NH USA
[11] Decis Sci Inst PIRE, Pawtucket, RI USA
基金
美国国家卫生研究院;
关键词
Alcohol Dependence; Levetiracetam; Keppra (R); Medications Development; Alcohol Use Disorder; WITHDRAWAL SYNDROME; DRUG; ANTICONVULSANTS; CONSUMPTION; TOPIRAMATE; GABAPENTIN; PROFILE;
D O I
10.1111/j.1530-0277.2011.01716.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
100404 [儿少卫生与妇幼保健学];
摘要
Background Despite advances in the development of medications to treat alcohol dependence, few medications have been approved by the U.S. Food and Drug Administration. The use of certain anticonvulsant medications has demonstrated potential efficacy in treating alcohol dependence. Previous research suggests that the anticonvulsant levetiracetam may be beneficial in an alcohol-dependent population of very heavy drinkers. Methods In this double-blind, randomized, placebo-controlled clinical trial, 130 alcohol-dependent patients who reported very heavy drinking were recruited across 5 clinical sites. Patients received either levetiracetam extended-release (XR) or placebo and a Brief Behavioral Compliance Enhancement Treatment intervention. Levetiracetam XR was titrated during the first 4 weeks to 2,000 mg/d. This target dose was maintained during weeks 5 through 14 and was tapered during weeks 15 and 16. Results No significant differences were detected between the levetiracetam XR and placebo groups in either the primary outcomes (percent heavy drinking days and percent subjects with no heavy drinking days) or in other secondary drinking outcomes. Treatment groups did not differ on a number of nondrinking outcomes, including depression, anxiety, mood, and quality of life. The only difference observed was in alcohol-related consequences. The levetiracetam XR treatment group showed significantly fewer consequences than did the placebo group during the maintenance period (p = 0.02). Levetiracetam XR was well tolerated, with fatigue being the only significantly elevated adverse event, compared with placebo (53% vs. 24%, respectively; p = 0.001). Conclusions This multisite clinical trial showed no efficacy for levetiracetam XR compared with placebo in reducing alcohol consumption in heavy drinking alcohol-dependent patients.
引用
收藏
页码:1421 / 1430
页数:10
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