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Double‐blind placebo‐controlled evaluation of the PROMETA™ protocol for methamphetamine dependence
Author(s) -
Ling Walter,
Shoptaw Steven,
Hillhouse Maureen,
Bholat Michelle A.,
Charuvastra Charles,
Heinzerling Keith,
Chim David,
An Jeffrey,
Dowling Patrick T.,
Doraimani Geetha
Publication year - 2012
Publication title -
addiction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.424
H-Index - 193
eISSN - 1360-0443
pISSN - 0965-2140
DOI - 10.1111/j.1360-0443.2011.03619.x
Subject(s) - methamphetamine , craving , placebo , medicine , flumazenil , anesthesia , adverse effect , gabapentin , clinical trial , cocaine dependence , benzodiazepine , addiction , psychiatry , alternative medicine , pathology , receptor
Aims To evaluate the efficacy and safety of the PROMETA™ Protocol for treating methamphetamine dependence. Design A double‐blind, placebo‐controlled 108‐day study with random assignment to one of two study conditions: active medication with flumazenil (2 mg infusions on days 1, 2, 3, 22, 23), gabapentin (1200 mg to day 40) and hydroxazine (50 mg to day 10) versus placebo medication (with active hydroxazine only). Setting Three substance abuse treatment clinics: two in‐patient, one out‐patient. Participants Treatment‐seeking, methamphetamine‐dependent adults ( n = 120). Measurements Primary outcome was percentage of urine samples testing negative for methamphetamine during the trial. Findings No statistically significant between‐group differences were detected in urine drug test results, craving, treatment retention or adverse events. Conclusions The PROMETA protocol, consisting of flumazenil, gabapentin and hydroxyzine, appears to be no more effective than placebo in reducing methamphetamine use, retaining patients in treatment or reducing methamphetamine craving.