Source:http://linkedlifedata.com/resource/pubmed/id/10669065
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2000-3-14
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pubmed:abstractText |
This study evaluated the efficacy of a combination tablet formulation of buprenorphine containing 8 mg of buprenorphine and 2 mg of naloxone for every other day treatment and whether increasing the daily maintenance dose was essential for maintaining an efficacious alternate-day treatment. Twenty-six opioid-dependent outpatients completing a 16-day baseline entered a double-blind, placebo-controlled, triple crossover trial. Twenty-one days of daily combination tablet administration were compared to two different 21-day periods of alternate-day buprenorphine administration where subjects received either 8 or 16 mg of the combination tablet every other day with placebo on the interposed day. Fifty-four percent (14/26) of subjects completed the study, but only two subjects dropped out during the 16-mg alternate-day condition. Rates of medication compliance, illicit opioid use and subject- and observer-rated measures of opioid effects did not distinguish daily from alternate-day treatments in subjects completing the study. However, pupillary diameter was significantly increased during 8-mg alternate-day compared to the 8-mg daily or 16-mg alternate-day treatment. These data replicate earlier findings describing the acceptability of alternate-day buprenorphine treatment using multiples of the daily maintenance dose and extend these findings by establishing the clinical efficacy of daily and alternate-day dosing regimens with the combination buprenorphine naloxone tablet. This study also suggests slightly improved outcomes during alternate-day treatment using multiples of the daily dose.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0376-8716
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
58
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
143-52
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10669065-Adult,
pubmed-meshheading:10669065-Analysis of Variance,
pubmed-meshheading:10669065-Buprenorphine,
pubmed-meshheading:10669065-Cross-Over Studies,
pubmed-meshheading:10669065-Double-Blind Method,
pubmed-meshheading:10669065-Drug Administration Schedule,
pubmed-meshheading:10669065-Drug Combinations,
pubmed-meshheading:10669065-Female,
pubmed-meshheading:10669065-Humans,
pubmed-meshheading:10669065-Male,
pubmed-meshheading:10669065-Naloxone,
pubmed-meshheading:10669065-Narcotic Antagonists,
pubmed-meshheading:10669065-Opioid-Related Disorders,
pubmed-meshheading:10669065-Pupil,
pubmed-meshheading:10669065-Questionnaires,
pubmed-meshheading:10669065-Statistics, Nonparametric,
pubmed-meshheading:10669065-Treatment Outcome
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pubmed:year |
2000
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pubmed:articleTitle |
Efficacy of daily and alternate-day dosing regimens with the combination buprenorphine-naloxone tablet.
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pubmed:affiliation |
Department of Psychiatry, University of Colorado School of Medicine, Vine Street Center, Denver 80206, USA. leslie.amass@uchsc.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Randomized Controlled Trial
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