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Exp Clin Psychopharmacol · Aug 1998
Randomized Controlled Trial Comparative Study Clinical TrialNicotine-mecamylamine treatment for smoking cessation: the role of pre-cessation therapy.
- J E Rose, F M Behm, and E C Westman.
- Nicotine Research Program, Veterans Affairs Medical Center, Durham, North Carolina 27705, USA. jerose@acpub.duke.edu
- Exp Clin Psychopharmacol. 1998 Aug 1;6(3):331-43.
AbstractThe nicotinic antagonist mecamylamine was evaluated in a randomized smoking cessation trial. Four groups of participants (n = 20 per group) received nicotine plus mecamylamine, nicotine alone, mecamylamine alone, or no drug for 4 weeks before cessation. After the quit-smoking date, all subjects received nicotine plus mecamylamine treatment for 6 weeks. Nicotine skin patches (21 mg/24 hr) and mecamylamine capsules (2.5-5.0 mg twice per day) were used. Precessation mecamylamine significantly prolonged the duration of continuous smoking abstinence; abstinence rates at the end of treatment were 47.5% with mecamylamine and 27.5% without mecamylamine. Nicotine + mecamylamine reduced ad lib smoking, smoking satisfaction, and craving more than either drug alone. Moreover, the orthostatic decrease in blood pressure caused by mecamylamine was offset by nicotine. Mecamylamine before smoking cessation may be an effective adjunct to nicotine patch therapy.
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