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临床试验/NCT00535002
NCT00535002已完成2 期

SCOR on Sex and Gender Factors Affecting Women's Health

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2007年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
112
试验地点
1
主要终点
Cocaine Craving

研究概览

简要总结

Stress and cues reminiscent of cocaine use promote craving and relapse in cocaine dependent individuals. In addition, there appears to be gender differences in determinants of relapse to drug use following abstinence in cocaine-dependent individuals. Therefore the purpose of the present study is to study the role of hormonal status on the response to cocaine-related cues with or without stress in cocaine-dependent women and men.

详细描述

Cocaine dependence is an insidious disease underscored by a strong propensity to relapse despite knowledge of the repercussions of continued drug-use. Stress and cocaine cues produce craving and ultimately relapse in cocaine dependent individuals. Pre-clinical research has demonstrated sex differences in response to cocaine-conditioned cues and cocaine-primed reinstatement, which correlates well with reduced plasma progesterone levels. Interestingly, this is consistent with a growing body of clinical literature indicating that progesterone may decrease the reinforcing properties of stimulants in women. Gender differences in the response to a social stressor and cocaine cues in cocaine-dependent individuals have been demonstrated in human laboratory studies, however, the interaction of stress and cues and the effect of hormonal status on response have not been explored. This study examines the role of hormonal status on the response to cocaine-related cues with or without a pharmacological stressor (yohimbine) in cocaine-dependent women and men. As a further integration of the research focus this study also explores the relationship between impulsivity and craving.

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 (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects must be able to provide informed consent and function at an intellectual level sufficient to allow accurate completion of all assessment instruments.
  • Subjects must consent to remain abstinent from all drugs of abuse (except nicotine) for a three-day period immediately prior to the CTRC admission. Nicotine dependence can affect HPA function (Baron et al., 1995) therefore it would be ideal to exclude subjects with nicotine use. Because of the high comorbidity of cocaine and nicotine dependence, this would seriously compromise the feasibility of recruitment. Individuals with alcohol dependence will be excluded. However because of the high comorbidity of alcohol use and cocaine dependence, individuals with alcohol abuse will be included. Also, due to the high comorbidity of cocaine and marijuana dependence, and limited evidence that marijuana use affects HPA function, subjects with marijuana dependence will be included.
  • Subjects with ADHD will be included. Because ADHD is commonly characterized by impulsivity, ADHD severity ratings will be determined and controlled for in data analysis.
  • Subjects must consent to random assignment.
  • Subjects must consent to outpatient admission to the CTRC and two overnight admissions to the Medical University Hospital.

排除标准

  • Women who are pregnant, nursing or of childbearing potential and not practicing an effective means of birth control.
  • Women with premenstrual dysphoric disorder as this may impact on the response to the stress test procedure (Woods et al., 1994).
  • Women receiving depot medroxyprogesterone acetate as a form of birth control.
  • Subjects with evidence of or a history of significant hematological, endocrine, cardiovascular, pulmonary, renal, gastrointestinal, or neurological disease including diabetes, as these conditions may affect physiological/subjective responses.
  • Subjects with Addison's disease, Cushing's disease or other diseases of the adrenal cortex likely to affect hormonal/neuroendocrine status.
  • Subjects with a history of or current psychotic disorder or bipolar affective disorder as these may interfere with subjective measurements.
  • Subjects with current major depressive disorder or post-traumatic stress disorder as these disorders are associated with characteristic changes in stress response.
  • Subjects with panic disorder, as yohimbine may precipitate panic attacks.
  • Subjects receiving synthetic glucocorticoid therapy, any exogenous steroid therapy, or treatment with other agents that interfere with hormonal measurements within one month of test session.
  • Subjects taking any psychotropic medications,antidepressants, opiates or opiate antagonists because these may affect test response. Subjects taking SSRI's will be included.
  • Subjects with any acute illness or fever. Individuals who otherwise meet study criteria will be rescheduled for evaluation for participation.
  • Subjects who are obese (BMI>35) as this may interfere with hormonal status.
  • Subjects who are unwilling or unable to maintain abstinence from alcohol and other drugs of abuse (except nicotine) for three days prior to the stress task procedure.
  • Subjects meeting DSM-IV criteria for substance dependence (other than nicotine, alcohol, marijuana or cocaine as appropriate) within the past 60 days.

研究组 & 干预措施

Cocaine Females, Yohimbine then Placebo

Other

Cocaine dependent females, received yohimbine day 1 and placebo day 2

干预措施: Yohimbine (Drug)

Cocaine Females, Yohimbine then Placebo

Other

Cocaine dependent females, received yohimbine day 1 and placebo day 2

干预措施: Placebo (Drug)

Cocaine Females, Placebo the Yohimbine

Other

Cocaine dependent females, received placebo day 1 and yohimbine day 2

干预措施: Yohimbine (Drug)

Cocaine Females, Placebo the Yohimbine

Other

Cocaine dependent females, received placebo day 1 and yohimbine day 2

干预措施: Placebo (Drug)

Cocaine Males, Yohimbine then Placebo

Other

Cocaine dependent males, received yohimbine day 1 and placebo day 2

干预措施: Yohimbine (Drug)

Cocaine Males, Yohimbine then Placebo

Other

Cocaine dependent males, received yohimbine day 1 and placebo day 2

干预措施: Placebo (Drug)

Cocaine Males, Placebo thenYohimbine

Other

Cocaine dependent males, received placebo day 1 and yohimbine day 2

干预措施: Yohimbine (Drug)

Cocaine Males, Placebo thenYohimbine

Other

Cocaine dependent males, received placebo day 1 and yohimbine day 2

干预措施: Placebo (Drug)

Control Females, Yohimbine then Placebo

Other

Non-dependent females, received yohimbine day 1 and placebo day 2

干预措施: Yohimbine (Drug)

Control Females, Yohimbine then Placebo

Other

Non-dependent females, received yohimbine day 1 and placebo day 2

干预措施: Placebo (Drug)

Control Females, Placebo then Yohimbine

Other

Non-dependent females, received placebo day 1 and yohimbine day 2

干预措施: Yohimbine (Drug)

Control Females, Placebo then Yohimbine

Other

Non-dependent females, received placebo day 1 and yohimbine day 2

干预措施: Placebo (Drug)

Control Males, Yohimbine then Placebo

Other

Non-dependent males, received yohimbine day 1 and placebo day 2

干预措施: Yohimbine (Drug)

Control Males, Yohimbine then Placebo

Other

Non-dependent males, received yohimbine day 1 and placebo day 2

干预措施: Placebo (Drug)

Control Males, Placebo then Yohimbine

Other

Non-dependent males, received placebo day 1 and yohimbine day 2

干预措施: Yohimbine (Drug)

Control Males, Placebo then Yohimbine

Other

Non-dependent males, received placebo day 1 and yohimbine day 2

干预措施: Placebo (Drug)

结局指标

主要结局

Cocaine Craving

时间窗: Post cocaine cue exposure

Cocaine-dependent participants were pre-treated with either yohimbine or placebo provided subjective ratings of cocaine craving immediately following cocaine cue exposure. The scale used was the Within Sessions Ratings Scales (Childress AR, McLellan AT, O'Brien CP (1986) Conditioned responses in a methadone population. A comparison of laboratory, clinic, and natural settings. Journal of Substance Abuse Treatment 3:173-179.) Craving was rated on a scale of 0-10 with 0 being Not At All and 10 being Extremely.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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