Effects of Inhaled Cannabis on Driving Performance

Alcohol Drinking Clinical Trial

Official title:

Effects of Inhaled Cannabis on Driving Performance

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01620177
• Other study ID #: 201109850
• Status: Completed
• Phase: N/A
• Start date: July 2012
• Est. completion date: March 2014

Study information

• Verified date: April 2018
• Source: University of Iowa
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to expand understanding of the effects of cannabis on driving performance with and without the presence of low levels of alcohol.

This project will involve the development a of a protocol and driving environment that is sensitive to the effects of cannabis on driving performance by building on prior driving situations used previously for testing the effects of alcohol on driving.

Description:

Individuals will be recruited who are currently users of cannabis and alcohol to participate in this study. They will undergo a physical exam at screening. There will be six study visits where the subject will arrive at the Clinical Research Unit(University of Iowa Hospitals & Clinics) the night before dosing. At each visit subjects will be receive one of the following six dosing regimens: placebo alcohol with placebo cannabis; placebo alcohol with low-dose cannabis, placebo alcohol with higher-dose of cannabis, low dose alcohol with placebo cannabis; low dose alcohol with low dose cannabis, low dose alcohol with higher-dose of cannabis. After dosing, participants will have provide saliva samples and blood drawn periodically to check cannabis levels and will complete a driving simulation. After completing the drive, additional saliva samples and blood draws will occur and participants will be monitored until it is safe to transport home.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 98
• Est. completion date: March 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years to 55 Years

Eligibility

Inclusion Criteria:

• Healthy adult (age 21-55) men and women, based on medical and psychological evaluation

• Currently valid unrestricted (except for vision correction) US driver's license

• Licensed driver for at least the past two years

• Drove at least 1300 miles in the past year, by self-report

• Live within an 80 mile radius of NADS

• Available for an overnight stay followed by a full-day study session for six sessions

• Must be considered a light or moderate drinker according to Quantity-Frequency-Variability Scale (QFV)

• Cannabis use with a minimum frequency averaging at least one day per quarter and no more than three days a week during the three months prior to study entry

• Peripheral veins suitable for repeated venipuncture and/or placement of an intravenous catheter

• Systolic blood pressure within a clinically normal range (120 ± 30 mmHg) and -diastolic blood pressure of 80 ± 20 mmHg..

• Good command of written and spoken English

• Female subjects with reproductive potential must agree to use (and/or have their partner use) one (1) acceptable method of birth control beginning at the screening visit throughout the study (including intervals between treatment periods/panels) and until 2 weeks after the last dose of study drug in the last treatment period. Acceptable methods of birth control include the following: intrauterine device (IUD-with or without local hormone release), diaphragm, spermicides, cervical cap, contraceptive sponge, oral contraceptives or condoms. Abstinence is an alternative lifestyle and subjects practicing abstinence may be included in the study.

Exclusion Criteria:

• Presence of any clinically significant illness, as detected by history, physical examination, and/or laboratory tests, that might influence driving performance (e.g., seizures, sleep apnea, narcolepsy, vertigo, chronic fatigue syndrome) or put the subject at increased risk of adverse events (e.g., cardiac arrhythmia, hypertension)

• History of a clinically significant adverse event associated with cannabis or alcohol intoxication

• Donation of more than 450 mL of blood within 14 days of study drug administration

• If female, pregnant or nursing

• Currently interested in or participating in drug abuse treatment, or participated in drug abuse treatment within 60 days preceding study enrollment

• Currently taking drugs that are contraindicated for use with study drugs

• Requires any special equipment to aid in driving (ex. pedal extensions, hand brake or throttle, spinner wheel knobs or other non-standard equipment)

• Significant history of motion sickness or demonstrates significant simulator sickness during practice drives at screening (SSQ). Subjects must have scores below the following values on the SSQ: Nausea < 21, Oculomotor <32, Disorientation < 15, and Total Score < 32.

• Current alcohol or cannabis use disorder, as identified by the Alcohol Use Disorders Identification Test for alcohol or Cannabis Use Disorders Identification Test for cannabis.

• History of any illness that, in the opinion of the study investigator, might confound the results of the study or pose an additional risk to the subject from study participation

• Prior participation in a driver impairment or distraction-related research study conducted at NADS that uses the same base drive.

Related Conditions & MeSH terms

• Alcohol Drinking
• Cannabis
• Marijuana Abuse

Intervention

Drug:
• Alcohol(oral) and placebo
Subjects will be dosed to an approximate peak BAC of 0.065%. Subjects will be tested on the decline such that subjects will be at or above the goal BAC (0.05%) throughout the drive
• Cannabis(THC)(Inhaled) and Placebo
Cannabis vapor is produced from 500 mg either placebo (0% THC), approximately 2.5-3.5% THC (low dose), or approximately 6.0-7.5% THC (high dose) bulk cannabis plant material to yield doses of approximately 0, 12.5-17.5, or 30-37.5 mg THC

Locations

Country	Name	City	State
United States	National Advanced Driving Simulator	Iowa City	Iowa

Sponsors (3)

Lead Sponsor	Collaborator
Gary R Gaffney	National Institute on Drug Abuse (NIDA), NHTSA

Country where clinical trial is conducted

United States, 

References & Publications (4)

Hartman RL, Brown TL, Milavetz G, Spurgin A, Gorelick DA, Gaffney G, Huestis MA. Controlled Cannabis Vaporizer Administration: Blood and Plasma Cannabinoids with and without Alcohol. Clin Chem. 2015 Jun;61(6):850-69. doi: 10.1373/clinchem.2015.238287. Epu — View Citation

Hartman RL, Brown TL, Milavetz G, Spurgin A, Gorelick DA, Gaffney G, Huestis MA. Controlled vaporized cannabis, with and without alcohol: subjective effects and oral fluid-blood cannabinoid relationships. Drug Test Anal. 2016 Jul;8(7):690-701. doi: 10.100 — View Citation

Hartman RL, Brown TL, Milavetz G, Spurgin A, Pierce RS, Gorelick DA, Gaffney G, Huestis MA. Cannabis effects on driving lateral control with and without alcohol. Drug Alcohol Depend. 2015 Sep 1;154:25-37. doi: 10.1016/j.drugalcdep.2015.06.015. Epub 2015 J — View Citation

Hartman RL, Brown TL, Milavetz G, Spurgin A, Pierce RS, Gorelick DA, Gaffney G, Huestis MA. Cannabis effects on driving longitudinal control with and without alcohol. J Appl Toxicol. 2016 Nov;36(11):1418-29. doi: 10.1002/jat.3295. Epub 2016 Feb 18. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Driving Performance	Measured by standard deviation of lane position. Metrics of driving performance were modeled using the SAS GLM Select function to identify changes in driver performance. Numbers represents coefficients on the regression equation such that this increase would be expected for every unit increase. A unit for THC is 1 ng/ml and a unit for BAC is 0.01% BAC. In understanding the regression coefficients, for THC the units for the coefficient would be expressed as cm per (ng/ml of THC), and for BrAC the units for the coefficient would be expressed as cm per (0.01% BrAC). The overall regression equation would be represented as SDLP = Intercept + Cthc x THC + Cbrac x BrAC. The coefficients indicate the strength of the effect on driving performance with higher coefficients indicating larger effects relative to the concentrations. Coefficients of zero indicate no effect or interactive effect.	Through entire drive, 0.5-1.3 hr post cannabis administration.
Secondary	THC Concentration in Plasma Sample	Measurement of THC concentration levels in plasma over the course of each visit compared to that of the other visits.	-0.7 hr, 0.25hr, 1.1 hr, 2 hr, 3 hr, 4.5 hr, 6 hr, 8 hr post cannabis administration
Secondary	THC Concentration Levels in Whole Blood	Measurement of THC concentration levels in whole blood over the course of each visit compared to that of the other visits.	-0.7 hr, 0.25hr, 1.1 hr, 2 hr, 3 hr, 4.5 hr, 6 hr, 8 hr post cannabis