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临床试验/NCT00124696
NCT00124696已完成1 期

Cocaethylene Substitution Therapy and Tolerance Induction in Treating Cocaine Dependence

National Institute on Drug Abuse (NIDA)2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2002年12月最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
8
试验地点
2
主要终点
Clinical physiological response to cocaine challenge - especially adverse effects measures

研究概览

简要总结

Cocaine has been cited as the primary drug threat in the United States. The purpose of this study is to determine if cocaethylene, used as a prototype drug, is a safe and effective treatment for cocaine dependence.

详细描述

Currently, there are no medications available to specifically treat cocaine addiction. Cocaethylene is an active metabolite of cocaine and has a similar chemical structure to cocaine. The purpose of this study is to determine whether substitution therapy with cocaethylene is a safe and effective treatment for cocaine dependence.

This double-blind, placebo-controlled trial will occur in 3 parts. In Part 1, the individual pharmacokinetics of an intravenous dose of cocaethylene will be determined in order to estimate individualized cocaethylene infusion rates and pharmacokinetic parameters. This will provide important information on how cocaethylene is processed by the body. In Part 2, an infusion of cocaethylene, producing a venous plasma concentration of 200 ng/ml, will be administered over an 8-hour period. Clinical monitoring and blood sampling will occur in order to determine the safety profile of cocaethylene. During Part 3, the ability of cocaethylene to modify the acute effects of intravenous cocaine will be determined. Cocaethylene will be administered in plasma concentrations of 0 ng/ml, 50 ng/ml, or 200 ng/ml over an 8-hour period. Participants will be randomly assigned to receive a challenge intravenous dose of cocaine (0.5 mg/kg or 1 mg/kg) or placebo at the 4-hour mark of cocaethylene infusion. Following the initial 8-hour period, cocaethylene infusion will be continued for an additional 5 hours. Behavioral and physiological measures will be collected throughout the study sessions at predetermined times to evaluate whether tolerance to cocaethylene develops. These measures will also help to determine whether cocaethylene modifies or produces tolerance to the effects of an acute dose of cocaine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Meets DSM-IV criteria for cocaine dependence
  • Cocaine use of at least 0.5 grams each week during the three months prior to enrollment, confirmed by a positive urine test for cocaine metabolite
  • Females are eligible if currently using adequate contraception, not planning to become pregnant, or surgically sterilized
  • Females of child-bearing potential must have a negative pregnancy test prior to study entry
  • Currently not physiologically dependent on alcohol, but may meet DSM-IV criteria for alcohol abuse or dependence

排除标准

  • Meets DSM-IV criteria for dependence on any drugs (other than nicotine or alcohol) within the year prior to enrollment
  • Currently abuses other substances such as opiates, sedative-hypnotics, or amphetamines (excluding marijuana or nicotine) more than twice a week
  • History of a serious medical illness or indication of a serious medical illness such as seizures, hypertension, heart disease, an abnormal ECG, anemia, diabetes, or abnormal blood flow sounds
  • Meets DSM-IV criteria for a current major mental disorder, including major depression, bipolar disorder, schizophrenia, schizophreniform disorder, schizoaffective disorder, mental retardation, or organic mental syndrome
  • Currently being treated with psychotropic medication
  • At risk for suicide, as determined by a psychiatrist
  • Greater than two times the normal level for liver or kidney function tests
  • Currently seeking treatment for drug abuse
  • Participants with liver function tests equal to or greater than three times the normal level will be discontinued from the study

结局指标

主要结局

Clinical physiological response to cocaine challenge - especially adverse effects measures

次要结局

未报告次要终点

研究者

申办方类型
Nih

研究点 (2)

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