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Completed

NCT Number: NCT03447353

Opiates and Benzodiazepines on Driving

The aim of this research is to assess drug effects (Xanax and Norco) on driving performance. Researchers will use the Alertness Memory Profiler (AMP) application to compare results to previous related studies.

This study continues a line of research designed to characterize the effects of common recreationally used prescription and illicit drugs with well known stimulant and sedating effects and their relationship to results from the Alertness Memory Profiler (AMP) that included a set of vigilance and memory tasks.

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Key information

Conditions

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

National Advanced Driving Simulator

Iowa City, Iowa, 52242, United States

About this study

This study uses EEG, EKG, computerized assessment, blood sampling, and driving simulation.

Individuals recruited will be normal, healthy individuals not currently taking the study drugs. The study will involve five visits, a screening visit as well as four dosing visits. The dosing visits will have a clean (double placebo) and three drugged visits (Xanax and Norco placebo, Xanax placebo and Norco, Xanax and Norco). The screening visit will last about two hours and will include drug and pregnancy testing as well as screening for physical/psychological health. Each of the dosing visits will last approximately five to six hours and will include sleep and food intake surveys, being dosed with study drugs or placebos, AMP assessments, a simulator drive, and wellness surveys. There will also be 4 mL blood sampling before dosing, before driving, and after driving.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy adult 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 5000 miles in the past year, by self-report
  • Live within a 60 mile radius of NADS
  • Available for five study sessions, with one being approximately 2 hours and four being approximately 5-6 hours
  • Peripheral veins suitable for repeated venipuncture
  • 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

  • Requires any special equipment to help drive, such as pedal extensions, hand brake or throttle, spinner wheel knobs, or other non-standard equipment
  • 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)
  • If female, pregnant or nursing
  • Currently taking drugs that are contraindicated for use with study drugs
  • 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.
  • 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

Treatment and study plan

Xanax 1Mg Tablet

Drug

Single dose on two of four visits, one in conjunction with 1 tab of 10mg/325mg Norco

Other names: Alprazolam

Norco 10Mg-325Mg Tablet

Drug

Single dose on two of the four study visits, one in conjunction with 1mg alprazolam

Other names: hydrocodone/acetaminophen

Placebo oral tablet

Drug

Single dose on two of the four study visits, double dose on one of the four study visits

Primary outcomes

  1. SDLP

    Time frame: over course of each simulator drive, approximately 35 minutes per visit

    Standard Deviation of Lane Position

    Standard deviation of lane position was analyzed using the SAS GLM function to identify changes in driver performance. Values represents means across the driving environments studied.

Secondary outcomes

  1. Lane Departures

    Time frame: over course of each simulator drive, approximately 35 minutes per visit

    Total number of lane departures per drive

    The total number of lane departures across the drive were analyzed using the SAS GLM procedure.

Sponsors and collaborators

Lead sponsor

Timothy L. Brown

Other

Registry information

Official study title

SAFER-SIM: Opiates and Benzodiazepines on Driving

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Feb 27, 2018
Registry last updated
Sep 27, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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