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临床试验/NCT04230460
NCT04230460已完成不适用

Cannabis Impairment Detection Application (CIDA)

Advanced Brain Monitoring, Inc.1 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2020年9月1日最近更新:
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
124
试验地点
1
主要终点
Driving Performance

研究概览

简要总结

Subjects will participate in a 4-visit study protocol in which they will be asked to complete a set of computerized tasks and a 45-minute simulated drive in a driving simulator. Subjects will be administered marijuana of varying pre-determined concentrations of delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD) during 3 of the visits and alcohol during one of the visits. Throughout the duration of each visit, brain activity will be measured noninvasively using an electroencephalogram (EEG) headset.

The purpose of this study is to:

  1. Further understand the effects of acute cannabis intoxication on driving performance in a driving simulator
  2. Develop and refine brain-based biomarkers of impairment due to acute cannabis intoxication

详细描述

At the University of Iowa, subjects who currently use cannabis recreationally (> once a month but < 5 times a week) will be recruited. They will then undergo a screening visit in which consent is obtained, questionnaires are given, and a physical exam is administered. They will then be scheduled for their next 3 (or 4 if participating in the alcohol arm), which will be at least one week apart. At each visit, in counter-balanced manner, subjects will be administered 500 mg of either placebo Marijuana (trace amounts of THC), high THC marijuana (7.5%), or very high THC marijuana (12.5%). All marijuana will be inhaled ad libitum via a Volcano® Digit vaporizer. Additionally, a subset of subjects will be asked to complete a fourth study visit that administers alcohol in place of cannabis. As subjects complete the third study visit and meet criteria for the alcohol arm, they will be invited to participate in the fourth study visit until eighteen subjects complete the study's alcohol arm. After drug administration, subjects will be asked to complete a set of computerized neurocognitive tasks (1 hour), followed by a simulated drive (45 minutes).

Throughout the duration of each visit, EEG will be collected. EEG is a non-invasive method of recording the electrical activity of the brain. Additionally, blood draws will be taken at pre-determined time points.

Finally, subjects will be monitored until the drug effects have subsided sufficiently to ensure it is safe to transport them home. Subjects will be transported home.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

University of Iowa: Triple (Participant, Investigator, Outcomes Assessor) blind

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

  • Men and women 18 to 50 years of age in good health (21 to 50 for alcohol arm)
  • Valid US driver's license and have been licensed driver for two years
  • Restrictions on driver's license limited to vision correction only
  • Drive at least three times per week
  • Must be able to drive without special or non-standard equipment
  • Must be able to attend three morning daytime study visits lasting approximately 5 to 6 hours
  • Must be willing to abstain from alcohol use in the day prior to their study appointments
  • Must be willing to abstain from use of their own cannabis while enrolled in the study
  • Live within 1-hour driving radius of National Advanced Driving Simulator (NADS)
  • Must currently use cannabis at least once every three months and no more than four times per week (must be current user)
  • Peripheral veins suitable for venipuncture
  • Blood pressure within clinically normal range
  • If invited to complete alcohol arm: Must be considered a light or moderate drinker according to Quantity-Frequency-Variability Scale (QFV) or, if a heavy drinker, not drink more than 1-2 times a week and not have a modal quantity of 5-6 drinks

排除标准

  • Females who are pregnant or test positive for pregnancy or are breastfeeding
  • Any known sleep disorders, or family history of sleep disorders
  • Any neurological or pulmonary disorders (or taking medications for such)
  • Any psychiatric disorder (or taking medications for such)
  • Any eating disorders
  • Recent (past 5 years) head injury, or older head injury with current symptoms
  • High blood pressure, Heart disease, diabetes, or history of stroke or taking medications to treat
  • Any known behavioral or attention disorder (or taking medications for such)
  • Untreated/Untreatable vision or auditory issues (because testing currently requires both senses)
  • Excessive tobacco use (more than 10 cigarettes a day)
  • Excessive caffeine use (5 or more servings per day)
  • Excessive alcohol (20 or more drinks per week)
  • Donation of 450 mL or more of blood in the two weeks preceding study drug administration
  • Regular use of pain medications other than over-the-counter
  • Any medication use that causes drowsiness or is contraindicated for driving
  • Use of prescription drugs not prescribed to them or illicit drugs other than cannabis
  • Propensity to motion sickness (more than 2-3 episodes where intensity is moderate or above)
  • History of substance abuse or substance addiction
  • Currently participating in or interested in drug abuse treatment, or participation in a program in past 60 days
  • Current cannabis use disorder or alcohol use disorder [as determined by scores on the Cannabis Use Disorder Identification Test (CUDIT) and Alcohol Use Disorder Identification Test (AUDIT)]

研究组 & 干预措施

0% THC/ 0% CBD

Placebo Comparator

干预措施: Cannabis (THC) (Inhaled) Placebo (Drug)

THC (5-10% [37.5 mg]) / Low CBD (<1% [2.5 mg])

Experimental

干预措施: Cannabis (High% THC) (Inhaled) (Drug)

THC (>10% [62.5 mg]) / Low CBD (<1% [2.5 mg])

Experimental

干预措施: Cannabis (Very High% THC) (Inhaled) (Drug)

0.065% BAC

Experimental

干预措施: Alcohol (oral) (Drug)

结局指标

主要结局

Driving Performance

时间窗: Through entire 45-minute drive, 0.5-1.3 hour post cannabis administration

Measured by standard deviation of lane position (SDLP, a gold standard metric of driving performance, O'Hanlon, 1984). This will provide a measure of general performance based on how well the driver maintains a consistent lane position. SDLP has been shown to be among the most important performance measures for evaluating the effects of psychophysiological changes due to impairment from medication use on driving performance (O'Hanlon, 1984).

EEG Measures

时间窗: Between -0.7 hours and 8 hours post cannabis administration

Changes in electroencephalogram (EEG) spectral power measures for Delta, Theta, Alpha, Beta, Gamma bands. EEG is sampled at 256 Hertz (Hz) and power spectral measures are calculated in one-second time intervals.

ECG Measures

时间窗: Between -0.7 hours and 8 hours post cannabis administration

Changes in heart rate as measured by electrocardiogram (ECG) (R-R interval). ECG is sampled at 256 Hz.

次要结局

  • Event-Related EEG Latency(From 0.5 hours to 1.5 hours post cannabis administration)
  • THC Concentration Levels in Whole Blood(-0.7 hour, 0.25 hour, 1.1 hour, 2 hour, 3 hour, 4.5 hour, 6 hour, 8 hour post cannabis administration)
  • THC Concentration in Plasma Sample(-0.7 hour, 0.25 hour, 1.1 hour, 2 hour, 3 hour, 4.5 hour, 6 hour, 8 hour post cannabis administration)
  • Event-Related EEG Amplitude(From 0.5 hours to 1.5 hours post cannabis administration)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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