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Addict Behav ; 20(4): 481-90, 1995.
Artigo em Inglês | MEDLINE | ID: mdl-7484329

RESUMO

This was a unblinded clinical trial of the stimulant methylphenidate (Ritalin) for nicotine withdrawal. Nineteen nicotine-dependent smokers received oral methylphenidate (30 mg target daily dosage) for 5 days following abrupt cessation. Tobacco withdrawal, Spielberger state anxiety, blood pressure, and pulse were measured at baseline, then serially for 7 days. Tobacco withdrawal and state anxiety increased significantly, but 12 (71%) of the 17 smokers who completed the study rated withdrawal relief "very define" and 13 (76%) rated this quit attempt "much easier than other times." Methylphenidate neither increased blood pressure nor blocked cessation-related pulse decrease and appears safe for this indication. Twelve (63%) of the enrolled smokers were confirmed abstinent at day 5. Methylphenidate effect on nicotine withdrawal should be studied in a placebo-controlled clinical trial.


Assuntos
Metilfenidato/administração & dosagem , Nicotina/efeitos adversos , Abandono do Hábito de Fumar , Síndrome de Abstinência a Substâncias/tratamento farmacológico , Administração Oral , Adulto , Relação Dose-Resposta a Droga , Esquema de Medicação , Feminino , Humanos , Masculino , Metilfenidato/efeitos adversos , Pessoa de Meia-Idade , Exame Neurológico/efeitos dos fármacos , Síndrome de Abstinência a Substâncias/diagnóstico
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