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临床试验/NCT01719497
NCT01719497已完成不适用

Imaging of Cannabinoid 1 Receptors Using [11C]OMAR and PET

Yale University1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2009年6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
已完成
入组人数
74
试验地点
1
主要终点
No outcome measures for this study, this is an imaging study only

研究概览

简要总结

The aim of the present study is to conduct a human trial of [C-11]OMAR, a new PET imaging agent for the brain cannabinoid type 1 receptors (CB1), to determine its pharmacokinetics and binding characteristics.

详细描述

This is a pilot, 2-part study to assess the kinetics of radioactivity in medically healthy subjects, subjects with alcohol dependency (AD), and obese subjects following the intravenous administration of the imaging agent [C-11]OMAR.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • Are overtly healthy males or females (other than AD or obesity), as determined by medical history and physical examination. Males and females with stable medical problems that, in the investigator's opinion, will not significantly alter the disposition of the drug, will not place the subject at increased risk by participating in the study, and will not interfere with interpretation of the data.
  • Are between the ages of 18 and 65 years, inclusive.
  • Have clinical laboratory test results within normal reference range for the population or investigator site, or results with acceptable deviations that are judged to be not clinically significant by the investigator. (Note: specific laboratory tests are listed in section 3.4)
  • Have arterial access sufficient to allow blood sampling as per the protocol.
  • Are reliable and willing to make themselves available for the duration of the study and are willing to follow study procedures.
  • Have given written informed consent approved by the ethical review board governing the site.

排除标准

  • Are currently enrolled in, or discontinued within the last [30 days] from, a clinical trial involving an off-label use of an investigational drug or device, or are concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study.
  • Current substance abuse (other than AD) including marijuana use, or severe systemic disease based on history and physical exam.
  • Laboratory tests with clinically significant abnormalities or positive urine toxicology screen. (Note: specific laboratory tests are listed in section 3.4)
  • Prior participation in other research protocols in the last year such that radiation exposure would exceed the annual limits.
  • Presence of ferromagnetic metal in the body or heart pacemaker.
  • Are persons who have previously completed or withdrawn from this study or any other study investigating [C-11]OMAR.
  • Regularly use known drugs of abuse (other than alcohol) within 30 days of the study and/or show positive findings on urinary drug screening.
  • Show evidence of human immunodeficiency virus (HIV) and/or positive human HIV antibodies.
  • Are women with a positive pregnancy test or women who are lactating.
  • Have a history of head trauma with prolonged loss of consciousness (>10 minutes), or any neurological condition including stroke or seizure (excluding a single childhood febrile seizure) or a history of migraine headaches
  • History of adverse drug reactions or intolerance to more than three types of systemically administered medications
  • Have used any prescription medication (except for oral contraceptives or hormone replacement therapy) or over-the-counter medication (including herbal remedies or diet aids) within 14 days of the imaging session. Multiple vitamins are specifically permitted
  • Have implanted or embedded metal objects or fragments in the head or body that would present a risk during the MRI scanning procedure, or have worked with ferrous metals either as a vocation or hobby (for example, as a sheet metal worker, welder, or machinist) in such a way that might have led to unknown, indwelling metal fragments that could cause injury if they moved in response to placement in the magnetic field
  • Have had exposure to ionizing radiation that in combination with the study tracer would result in a cumulative exposure that exceeds recommended exposure limits

研究组 & 干预措施

Alcohol

Subjects diagnosed with alcohol dependence

干预措施: [C-11]OMAR (Drug)

Obese

Subjects diagnosed with obesity

干预措施: [C-11]OMAR (Drug)

High Stress

Subjects diagnosed with high stress

干预措施: [C-11]OMAR (Drug)

Healthy

Subjects deemed medically healthy

干预措施: [C-11]OMAR (Drug)

结局指标

主要结局

No outcome measures for this study, this is an imaging study only

时间窗: Upon study completion

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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