A randomized, placebo-controlled trial of sustained-release dextroamphetamine for treatment of methamphetamine addiction
Sixty treatment-seeking individuals with methamphetamine (MA) dependence entered a randomized, placebo-controlled, double-blind clinical trial of oral dextroamphetamine (d-AMP) as a replacement therapy for MA dependence. The subjects took 60 mg sustained-release d-AMP for 8 weeks, during which time...
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Published in | Clinical pharmacology and therapeutics Vol. 89; no. 2; p. 276 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
01.02.2011
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Abstract | Sixty treatment-seeking individuals with methamphetamine (MA) dependence entered a randomized, placebo-controlled, double-blind clinical trial of oral dextroamphetamine (d-AMP) as a replacement therapy for MA dependence. The subjects took 60 mg sustained-release d-AMP for 8 weeks, during which time they received eight 50-min sessions of individual psychotherapy. Adverse events and urine toxicology for MA were assessed two times a week. There were no serious adverse events. Urine samples containing <1,000 ng/ml of MA were classified as negative for MA. The MA-negative scores in the d-AMP group (3.1 ± SD 4.6) were no higher than those in the placebo group (3.3 ± SD 5.3; P > 0.05). However, withdrawal and craving scores were significantly lower in the d-AMP group (P < 0.05 for both). Although subjects taking d-AMP did not reduce their use of MA, the significant reductions observed in withdrawal and craving scores in this group support the need for further exploration of d-AMP as a pharmacologic intervention for MA dependence, possibly at higher doses. |
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AbstractList | Sixty treatment-seeking individuals with methamphetamine (MA) dependence entered a randomized, placebo-controlled, double-blind clinical trial of oral dextroamphetamine (d-AMP) as a replacement therapy for MA dependence. The subjects took 60 mg sustained-release d-AMP for 8 weeks, during which time they received eight 50-min sessions of individual psychotherapy. Adverse events and urine toxicology for MA were assessed two times a week. There were no serious adverse events. Urine samples containing <1,000 ng/ml of MA were classified as negative for MA. The MA-negative scores in the d-AMP group (3.1 ± SD 4.6) were no higher than those in the placebo group (3.3 ± SD 5.3; P > 0.05). However, withdrawal and craving scores were significantly lower in the d-AMP group (P < 0.05 for both). Although subjects taking d-AMP did not reduce their use of MA, the significant reductions observed in withdrawal and craving scores in this group support the need for further exploration of d-AMP as a pharmacologic intervention for MA dependence, possibly at higher doses. |
Author | Galloway, G P Flower, K Fiske, L A Siegrist, J D Li, L Chen, C Y A Polcin, D Coyle, J R Mendelson, J Buscemi, R Baggott, M J |
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SubjectTerms | Adult Amphetamine-Related Disorders - drug therapy Delayed-Action Preparations Dextroamphetamine - administration & dosage Dextroamphetamine - adverse effects Double-Blind Method Female Humans Male Medication Adherence Methamphetamine - adverse effects |
Title | A randomized, placebo-controlled trial of sustained-release dextroamphetamine for treatment of methamphetamine addiction |
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