A double blind, placebo controlled trial of modafinil for the treatment of cocaine dependence without co-morbid alcohol dependence

•This was a double blind placebo controlled trial of modafinil for cocaine dependence.•It involved 94 subjects treated with 300mg of modafinil or placebo daily for 8 weeks.•Modafinil treated subjects were more likely to achieve cocaine abstinence.•Modafinil treated subjects were more likely to repor...

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Published inDrug and alcohol dependence Vol. 155; pp. 105 - 110
Main Authors Kampman, Kyle M., Lynch, Kevin G., Pettinati, Helen M., Spratt, Kelly, Wierzbicki, Michael R., Dackis, Charles, O’Brien, Charles P.
Format Journal Article
LanguageEnglish
Published Ireland Elsevier Ireland Ltd 01.10.2015
Subjects
Online AccessGet full text
ISSN0376-8716
1879-0046
1879-0046
DOI10.1016/j.drugalcdep.2015.08.005

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Abstract •This was a double blind placebo controlled trial of modafinil for cocaine dependence.•It involved 94 subjects treated with 300mg of modafinil or placebo daily for 8 weeks.•Modafinil treated subjects were more likely to achieve cocaine abstinence.•Modafinil treated subjects were more likely to report very low levels of cocaine craving.•Modafinil treated subjects were more likely to rate themselves very much improved. Modafinil is a medication approved for narcolepsy and shift work sleep disorder. It has both dopaminergic and glutamatergic activity that could be useful for the treatment of cocaine dependence. Modafinil has reduced cocaine subjective effects and cocaine self-administration in human laboratory trials and has reduced cocaine use in cocaine dependent patients in some clinical trials. This was an 8-week, double blind, placebo controlled clinical trial involving 94 cocaine dependent subjects. Subjects received 300mg of modafinil or identical placebo daily along with weekly individual therapy. The primary outcome measure was cocaine use measured by self-report, and confirmed by twice weekly urine benzoylecgonine tests (UBT). Additional outcome measures included cocaine craving measured by the Brief Substance Craving Scale and global improvement measured by the Clinical Global Impression Scale (CGI). The odds ratio (OR) in favor of abstinence for modafinil vs. placebo was 2.54 (p=. 03) and modafinil-treated subjects were significantly more likely than placebo-treated subjects to be abstinent from cocaine during the last 3 weeks of the trial, 23% vs. 9%, χ2=3.9, p<.05. Modafinil treated subjects were more likely to report very low levels of cocaine craving intensity and duration on the Brief Substance Craving Scale (OR=2.04, p=.03 and OR 1.06, p=.03 respectively). Modafinil-treated subjects were also more likely than placebo-treated subjects to rate themselves as “very much improved” on the CGI (OR=2.69, p=.03). Modafinil may be an efficacious treatment for cocaine dependence.
AbstractList Highlights • This was a double blind placebo controlled trial of modafinil for cocaine dependence. • It involved 94 subjects treated with 300 mg of modafinil or placebo daily for 8 weeks. • Modafinil treated subjects were more likely to achieve cocaine abstinence. • Modafinil treated subjects were more likely to report very low levels of cocaine craving. • Modafinil treated subjects were more likely to rate themselves very much improved.
Modafinil is a medication approved for narcolepsy and shift work sleep disorder. It has both dopaminergic and glutamatergic activity that could be useful for the treatment of cocaine dependence. Modafinil has reduced cocaine subjective effects and cocaine self-administration in human laboratory trials and has reduced cocaine use in cocaine dependent patients in some clinical trials. This was an 8-week, double blind, placebo controlled clinical trial involving 94 cocaine dependent subjects. Subjects received 300mg of modafinil or identical placebo daily along with weekly individual therapy. The primary outcome measure was cocaine use measured by self-report, and confirmed by twice weekly urine benzoylecgonine tests (UBT). Additional outcome measures included cocaine craving measured by the Brief Substance Craving Scale and global improvement measured by the Clinical Global Impression Scale (CGI). The odds ratio (OR) in favor of abstinence for modafinil vs. placebo was 2.54 (p=. 03) and modafinil-treated subjects were significantly more likely than placebo-treated subjects to be abstinent from cocaine during the last 3 weeks of the trial, 23% vs. 9%, χ(2)=3.9, p<.05. Modafinil treated subjects were more likely to report very low levels of cocaine craving intensity and duration on the Brief Substance Craving Scale (OR=2.04, p=.03 and OR 1.06, p=.03 respectively). Modafinil-treated subjects were also more likely than placebo-treated subjects to rate themselves as "very much improved" on the CGI (OR=2.69, p=.03). Modafinil may be an efficacious treatment for cocaine dependence.
Modafinil is a medication approved for narcolepsy and shift work sleep disorder. It has both dopaminergic and glutamatergic activity that could be useful for the treatment of cocaine dependence. Modafinil has reduced cocaine subjective effects and cocaine self-administration in human laboratory trials and has reduced cocaine use in cocaine dependent patients in some clinical trials.BACKGROUNDModafinil is a medication approved for narcolepsy and shift work sleep disorder. It has both dopaminergic and glutamatergic activity that could be useful for the treatment of cocaine dependence. Modafinil has reduced cocaine subjective effects and cocaine self-administration in human laboratory trials and has reduced cocaine use in cocaine dependent patients in some clinical trials.This was an 8-week, double blind, placebo controlled clinical trial involving 94 cocaine dependent subjects. Subjects received 300mg of modafinil or identical placebo daily along with weekly individual therapy. The primary outcome measure was cocaine use measured by self-report, and confirmed by twice weekly urine benzoylecgonine tests (UBT). Additional outcome measures included cocaine craving measured by the Brief Substance Craving Scale and global improvement measured by the Clinical Global Impression Scale (CGI).METHODSThis was an 8-week, double blind, placebo controlled clinical trial involving 94 cocaine dependent subjects. Subjects received 300mg of modafinil or identical placebo daily along with weekly individual therapy. The primary outcome measure was cocaine use measured by self-report, and confirmed by twice weekly urine benzoylecgonine tests (UBT). Additional outcome measures included cocaine craving measured by the Brief Substance Craving Scale and global improvement measured by the Clinical Global Impression Scale (CGI).The odds ratio (OR) in favor of abstinence for modafinil vs. placebo was 2.54 (p=. 03) and modafinil-treated subjects were significantly more likely than placebo-treated subjects to be abstinent from cocaine during the last 3 weeks of the trial, 23% vs. 9%, χ(2)=3.9, p<.05. Modafinil treated subjects were more likely to report very low levels of cocaine craving intensity and duration on the Brief Substance Craving Scale (OR=2.04, p=.03 and OR 1.06, p=.03 respectively). Modafinil-treated subjects were also more likely than placebo-treated subjects to rate themselves as "very much improved" on the CGI (OR=2.69, p=.03).RESULTSThe odds ratio (OR) in favor of abstinence for modafinil vs. placebo was 2.54 (p=. 03) and modafinil-treated subjects were significantly more likely than placebo-treated subjects to be abstinent from cocaine during the last 3 weeks of the trial, 23% vs. 9%, χ(2)=3.9, p<.05. Modafinil treated subjects were more likely to report very low levels of cocaine craving intensity and duration on the Brief Substance Craving Scale (OR=2.04, p=.03 and OR 1.06, p=.03 respectively). Modafinil-treated subjects were also more likely than placebo-treated subjects to rate themselves as "very much improved" on the CGI (OR=2.69, p=.03).Modafinil may be an efficacious treatment for cocaine dependence.CONCLUSIONModafinil may be an efficacious treatment for cocaine dependence.
•This was a double blind placebo controlled trial of modafinil for cocaine dependence.•It involved 94 subjects treated with 300mg of modafinil or placebo daily for 8 weeks.•Modafinil treated subjects were more likely to achieve cocaine abstinence.•Modafinil treated subjects were more likely to report very low levels of cocaine craving.•Modafinil treated subjects were more likely to rate themselves very much improved. Modafinil is a medication approved for narcolepsy and shift work sleep disorder. It has both dopaminergic and glutamatergic activity that could be useful for the treatment of cocaine dependence. Modafinil has reduced cocaine subjective effects and cocaine self-administration in human laboratory trials and has reduced cocaine use in cocaine dependent patients in some clinical trials. This was an 8-week, double blind, placebo controlled clinical trial involving 94 cocaine dependent subjects. Subjects received 300mg of modafinil or identical placebo daily along with weekly individual therapy. The primary outcome measure was cocaine use measured by self-report, and confirmed by twice weekly urine benzoylecgonine tests (UBT). Additional outcome measures included cocaine craving measured by the Brief Substance Craving Scale and global improvement measured by the Clinical Global Impression Scale (CGI). The odds ratio (OR) in favor of abstinence for modafinil vs. placebo was 2.54 (p=. 03) and modafinil-treated subjects were significantly more likely than placebo-treated subjects to be abstinent from cocaine during the last 3 weeks of the trial, 23% vs. 9%, χ2=3.9, p<.05. Modafinil treated subjects were more likely to report very low levels of cocaine craving intensity and duration on the Brief Substance Craving Scale (OR=2.04, p=.03 and OR 1.06, p=.03 respectively). Modafinil-treated subjects were also more likely than placebo-treated subjects to rate themselves as “very much improved” on the CGI (OR=2.69, p=.03). Modafinil may be an efficacious treatment for cocaine dependence.
Author Lynch, Kevin G.
Kampman, Kyle M.
Pettinati, Helen M.
Wierzbicki, Michael R.
Dackis, Charles
Spratt, Kelly
O’Brien, Charles P.
AuthorAffiliation a Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3900 Chestnut Street, Philadelphia, PA, USA, 19104
c Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA, USA, 19104
b Department of Medicine, Perelman School of Medicine, University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA, USA, 19104
AuthorAffiliation_xml – name: a Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3900 Chestnut Street, Philadelphia, PA, USA, 19104
– name: c Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA, USA, 19104
– name: b Department of Medicine, Perelman School of Medicine, University of Pennsylvania, 3400 Spruce Street, Philadelphia, PA, USA, 19104
Author_xml – sequence: 1
  givenname: Kyle M.
  surname: Kampman
  fullname: Kampman, Kyle M.
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  organization: Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3900 Chestnut Street, Philadelphia, PA 19104, USA
– sequence: 2
  givenname: Kevin G.
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  organization: Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3900 Chestnut Street, Philadelphia, PA 19104, USA
– sequence: 3
  givenname: Helen M.
  surname: Pettinati
  fullname: Pettinati, Helen M.
  organization: Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3900 Chestnut Street, Philadelphia, PA 19104, USA
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  givenname: Michael R.
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– sequence: 6
  givenname: Charles
  surname: Dackis
  fullname: Dackis, Charles
  organization: Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3900 Chestnut Street, Philadelphia, PA 19104, USA
– sequence: 7
  givenname: Charles P.
  surname: O’Brien
  fullname: O’Brien, Charles P.
  organization: Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, 3900 Chestnut Street, Philadelphia, PA 19104, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26320827$$D View this record in MEDLINE/PubMed
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Keywords Alcohol
Clinical trial
Cocaine
Modafinil
Placebo
Language English
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Snippet •This was a double blind placebo controlled trial of modafinil for cocaine dependence.•It involved 94 subjects treated with 300mg of modafinil or placebo daily...
Highlights • This was a double blind placebo controlled trial of modafinil for cocaine dependence. • It involved 94 subjects treated with 300 mg of modafinil...
Modafinil is a medication approved for narcolepsy and shift work sleep disorder. It has both dopaminergic and glutamatergic activity that could be useful for...
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StartPage 105
SubjectTerms Adolescent
Adult
Alcohol
Alcoholism - epidemiology
Benzhydryl Compounds - adverse effects
Benzhydryl Compounds - therapeutic use
Clinical trial
Cocaine
Cocaine - analogs & derivatives
Cocaine - urine
Cocaine-Related Disorders - drug therapy
Cocaine-Related Disorders - epidemiology
Cocaine-Related Disorders - urine
Cognitive Therapy
Combined Modality Therapy
Craving - drug effects
Double-Blind Method
Female
Humans
Male
Medication Adherence - statistics & numerical data
Middle Aged
Modafinil
Patient Compliance - statistics & numerical data
Placebo
Psychiatric Status Rating Scales
Psychiatry
Treatment Outcome
Young Adult
Title A double blind, placebo controlled trial of modafinil for the treatment of cocaine dependence without co-morbid alcohol dependence
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0376871615015963
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https://dx.doi.org/10.1016/j.drugalcdep.2015.08.005
https://www.ncbi.nlm.nih.gov/pubmed/26320827
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https://pubmed.ncbi.nlm.nih.gov/PMC4582003
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