Evidence map›Paper›PMID 18796184›Full record

Trial reportThe international journal of neuropsychopharmacology2009

Dose-dependent reduction of hazardous alcohol use in a placebo-controlled trial of naltrexone for smoking cessation.

Stephanie S O'Malley, Suchitra Krishnan-Sarin, Sherry A McKee, Robert F Leeman, Ned L Cooney, Boris Meandzija, Ran Wu, Robert W Makuch

Open access · bronzeAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The international journal of neuropsychopharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Opioid antagonists for smoking cessation.The Cochrane database of systematic reviews · 2013
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  6. Predictors of Naltrexone Response in a Randomized Trial: Reward-Related Brain Activation, OPRM1 Genotype, and Smoking Status.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Stephanie S O'MalleyDepartment of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA. stephanie.omalley@yale.edu
Suchitra Krishnan-Sarin
Sherry A McKee
Robert F Leeman
Ned L Cooney
Boris Meandzija
Ran Wu
Robert W Makuch
Yale University · US

Funding

Tobacco Dependence &Risk Factors for Treatment FailureP50AA015632 · NIAAA · YALE UNIVERSITY · PI MCKEE, SHERRY ANN · 2004 to 2008
$9.2M
TOBACCO DEPENDENCE AND RISK FACTORS FOR TREATMENT FAILURP50DA013334 · NIDA · YALE UNIVERSITY · PI O'MALLEY, STEPHANIE S · 1999 to 2003
$8.0M
FIELD STUDY OF SMOKING CESSATION IN ALCOHOLISM TREATMENTR01AA011197 · NIAAA · YALE UNIVERSITY · PI COONEY, NED L · 1997 to 2011
$4.3M
ENHANCED ALCOHOLISM TREATMENT STRATEGIES--NALTREXONEK02AA000171 · NIAAA · YALE UNIVERSITY · PI O'MALLEY, STEPHANIE S · 1993 to 2003
$430k
NIAAA NIH HHS K02 AA000171NIAAA NIH HHS K02-AA00171NIAAA NIH HHS P50 AA015632NIAAA NIH HHS P50-AA-15632NIAAA NIH HHS R01 AA011197NIAAA NIH HHS R01-AA11197NIDA NIH HHS P50 DA013334NIDA NIH HHS P50-DA-13334
6 · The paper itself

Abstract

The opiate antagonist naltrexone (Ntx) has demonstrated efficacy in the treatment of alcohol dependence and as a component of treatment to reduce heavy drinking. At present, there are no published dose-ranging clinical trials of the oral preparation for treatment of problem drinking. The present study evaluated the effects of Ntx on alcohol use among the subset of hazardous drinkers (n=102) who participated in a placebo-controlled, dose-ranging trial of oral Ntx (25-mg, 50-mg and 100-mg doses) combined with open-label transdermal nicotine patch for enhancing smoking cessation. On the primary outcome--no hazardous drinking (drinking that exceeded weekly or daily limits) during treatment--25 mg and 50 mg Ntx were superior to placebo (each p<0.05). These findings remained after controlling for baseline predictors or smoking abstinence during treatment. Time to remission of hazardous drinking was examined as a secondary outcome with definitions of hazardous drinking based on weekly limits, daily limits and the combination of weekly and daily limits and the results were consistent with the primary findings. In conclusion, the findings suggest that Ntx can reduce the risk of hazardous drinking in smokers who are not seeking or receiving alcohol treatment, providing strong evidence for the pharmacological effects of Ntx on drinking. This effect appears to favour lower doses that may be better tolerated and less expensive than the higher 100-mg dose. Given its efficacy and favourable side-effect profile, the 25-mg dose should be considered for future studies of combination therapy.

Indexed as

AdultAlcohol DrinkingAlcoholismDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedNaltrexoneSmokingSmoking CessationNaltrexone

Identifiers

PMID18796184
PMCPMC3094855
OpenAlexW2145159339

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.