跳至主要内容
临床试验/NCT02152670
NCT02152670终止不适用

Understanding Dopamine Mechanisms in Cocaine Addiction Using AMPT and Methylphenidate With [11C]RAC/[11C]PHNO PET

Yale University1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2014年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
1
主要终点
BPND

研究概览

简要总结

Studies using positron emission tomography (PET) have been used with great success in demonstrating specific abnormalities in several facets of dopaminergic system function in human populations (Narendran and Martinez 2009). Among the first, most consistent, and broadly replicated of such findings in drug- (including cocaine) dependent individuals has been the reduction in subcortical (striatal) D2/3 receptors as imaged, most commonly, by the reversible, non-selective, D2/3 receptor antagonist radiotracer, [11C]raclopride. Certain dissociations on D2/3 availability by radioligand ([11C]raclopride vs. [11C]PHNO) and by brain region (striatum vs. SN; terminal vs. somatodendritic, respectively) are poorly understood in relationship to prior antagonist tracer results. In the current study the investigators will use pharmacological interventions (AMPT and methylphenidate) with both antagonist and agonist radiotracers to experimentally reconcile these discordant findings and clarify potential mechanistic inter-relationships.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Factorial
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • age 18 - 50 years,
  • voluntary, written, informed consent,
  • physically healthy by medical history, physical, neurological, ECG, and laboratory examinations,
  • for females, non-lactating, no longer of child-bearing potential (or agree to practice effective contraception during the study), and a negative serum pregnancy (B-HCG) test.
  • English speaking
  • No other major Axis DSM-IV diagnosis present, besides required as below
  • Inclusion criteria for cocaine dependent:
  • DSM-IV criteria for Cocaine Abuse (305.60) or Cocaine Dependence (304.20)
  • recent street cocaine use,
  • intravenous and/or smoked (crack/ freebase) use,
  • positive urine toxicology screen for cocaine,
  • Inclusion criteria for healthy controls:
  • No current, or history of, any DSM-IV diagnosis
  • No first-degree relative with history of psychotic, mood, or anxiety disorder

排除标准

  • medical contraindications to AMPT administration (e.g., known sensitivity/reaction to AMPT);
  • medical contraindications to MPH administration (e.g., history of cardiac problems, seizures, etc.)
  • drug or alcohol dependence (except nicotine),
  • a primary major DSM-IV psychiatric diagnosis (schizophrenia, bipolar disorder, etc.), unrelated to cocaine or pathological gambling
  • positive answers on the cardiac screening questionnaire that may place the subject at higher risk, as determined by cardiologist review of both the questionnaire responses and screening ECG
  • current use of psychotropic and/or potentially psychoactive prescription medication,
  • physical or laboratory (B-HCG) evidence of pregnancy,
  • clotting disorders or recent anticoagulant therapy,
  • MRI-incompatible implants and other contraindications for MRI (i.e., aneurysm clip, metal fragments, internal electrical devices such as a cochlear implant, spinal cord stimulator or pacemaker),
  • history of claustrophobia or feeling of inability to lie still on his back for the PET or MRI scans,
  • history of prior radiation exposure for research purposes within the past year such that participation in this study would place them over Radioactive Drug Research Committee (RDRC) limits for annual radiation exposure. This guideline is an effective dose of 5 rem received per year.
  • donation or loss of 550 mL of blood or more (including plasmapheresis) or receipt of a transfusion of any blood product within 8 weeks prior to the first dose of study drug.
  • use any prescription medications and/or over-the-counter medications, vitamins and/or herbal supplements within 2 weeks prior to study and for the duration of the study without approval from the study doctor.
  • eat grapefruit or grapefruit products, and drink alcohol, and anything containing caffeine 3 days before study and during study
  • For CD subjects, < 1 year of cocaine dependence, .
  • Subjects with current, past, or anticipated exposure to radiation in the workplace.

研究组 & 干预措施

Baseline

Experimental

Subjects will receive 2 baseline PET scans with the radioligands (11C)(+)PHNO and (11C)(+)raclopride

干预措施: [11C]PHNO (Other)

Baseline

Experimental

Subjects will receive 2 baseline PET scans with the radioligands (11C)(+)PHNO and (11C)(+)raclopride

干预措施: [11C]raclopride (Other)

Dopamine Release

Experimental

Subjects will receive 1 PET scan following a PO dose of 60mg of methylphenidate to facilitate dopamine release with the radioligand (11C)(+)PHNO

干预措施: Methylphenidate (Drug)

Dopamine Release

Experimental

Subjects will receive 1 PET scan following a PO dose of 60mg of methylphenidate to facilitate dopamine release with the radioligand (11C)(+)PHNO

干预措施: [11C]PHNO (Other)

Endogenous Dopamine

Experimental

Subjects will receive 2 PET scans following 48 hours of dopamine depletion via AMPT with the radioligands (11C)(+)PHNO and (11C)(+)raclopride

干预措施: Alpha Methyl Para Tyrosine (AMPT) (Drug)

Endogenous Dopamine

Experimental

Subjects will receive 2 PET scans following 48 hours of dopamine depletion via AMPT with the radioligands (11C)(+)PHNO and (11C)(+)raclopride

干预措施: [11C]PHNO (Other)

Endogenous Dopamine

Experimental

Subjects will receive 2 PET scans following 48 hours of dopamine depletion via AMPT with the radioligands (11C)(+)PHNO and (11C)(+)raclopride

干预措施: [11C]raclopride (Other)

结局指标

主要结局

BPND

时间窗: 2 weeks

BPND is a measure of dopamine receptor availability

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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