Table 2.
GABA agents
Pharmacological agents | Study design Sample characteristics | Outcomes | Results | Main limitations | References |
---|---|---|---|---|---|
Baclofen (60 mg day−1) | 16-week, randomized, placebo-controlled, double-blind trial with 3 arms including gabapentin and placebo as well as baclofen 25 methamphetamine dependent patients Primary route of use: smoking | Primary outcomeMethamphetamine use (urine drug tests) Secondary outcomesTreatment retention, depressive symptoms, methamphetamine cravings, adverse events | Not effective in reducing methamphetamine use Small treatment effect relative to placebo among participants who reported taking a higher percentage of study medication (post hoc analyses) | Small sample size Increasing attrition of the participants biological measures of medication adherence not performed | [80] |
Gabapentin (2400 mg day−1) | 16-week, randomized, placebo-controlled, double-blind trial with 3 arms including baclofen and placebo as well as gabapentin 26 methamphetamine dependent patients Primary route of use: smoking | Primary outcomeMethamphetamine use (urine drug tests) Secondary outcomesTreatment retention, depressive symptoms, methamphetamine cravings, adverse events | Not effective in reducing methamphetamine use | Small sample size Increasing attrition of the participants biological measures of medication adherence not performed | [80] |
Vigabatrin (from 1 to 3 g day−1) | 9-week open-label safety study 28 methamphetamine and/or cocaine dependent patients | Primary outcomesChange of visual fields, visual acuity, ocular adverse effects Secondary outcomesMethamphetamine use | No ophthalmologic adverse effects Decrease of methamphetamine use | Small sample size Open label design No control group High drop-out rate (approximately 50%) | [83] |
Vigabatrin (from 1.5 to 3 g day−1) | 9-week open-label safety study 30 methamphetamine and/or cocaine dependent patients | Primary outcomesChange of visual fields, visual acuity, ocular adverse effects Secondary outcomesMethamphetamine use | No ophthalmologic adverse effects Decrease of methamphetamine use | Small sample size Open label design No control group High drop-out rate (approximately 50%) | [83] |