NCT02404688

Brief Summary

The overarching goal of this study is to characterize the effects of ethanol and cannabinoids on simulated driving and related cognition.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P50-P75 for phase_1

Timeline
7mo left

Started Dec 2015

Longer than P75 for phase_1

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress95%
Dec 2015Dec 2026

First Submitted

Initial submission to the registry

March 26, 2015

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 31, 2015

Completed
8 months until next milestone

Study Start

First participant enrolled

December 1, 2015

Completed
11 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

April 29, 2026

Status Verified

April 1, 2026

Enrollment Period

11 years

First QC Date

March 26, 2015

Last Update Submit

April 23, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Road Tracking Error

    changes in road tracking errors between timepoints to assess the effects of alcohol and THC on road tracking errors.

    baseline, +20, +50, +120, +180 mins after start of alcohol and THC infusion

Secondary Outcomes (6)

  • Biphasic Alcohol Effects Scale (BAES)

    baseline, +20, +50, +120, +180, +240 mins after start of alcohol and THC infusion

  • Visual Analog Scale (VAS)

    baseline, +20, +50, +120, +180 mins after start of alcohol and THC infusion

  • Cognitive Test Battery

    +40 mins after start of alcohol and THC infusion

  • Willingness to Drive Scale

    baseline, +20, +50, +120, +180 mins after start of alcohol and THC infusion

  • Number of Joints Scale

    baseline, +20, +50, +120, +180 mins after start of alcohol and THC infusion

  • +1 more secondary outcomes

Study Arms (4)

Active THC and Placebo Ethanol

EXPERIMENTAL
Drug: Active delta-9-THCDrug: Placebo

Active THC and Active Ethanol

EXPERIMENTAL
Drug: Active delta-9-THCDrug: Active Ethanol

Placebo THC and Active Ethanol

EXPERIMENTAL
Drug: PlaceboDrug: Active Ethanol

Placebo THC and Placebo Ethanol

PLACEBO COMPARATOR
Drug: Placebo

Interventions

Low dose (0.015 mg/kg = 1.05 mg in a 70 kg individual) THC, dissolved in alcohol. This dose is roughly equivalent to smoking approximately 1/4 of a marijuana cigarette, or "joint". Administered over 20 minutes.

Active THC and Active EthanolActive THC and Placebo Ethanol

Target BrAC of 0.04% reached over 20 minutes and then clamped to maintain this dose for an additional 60 minutes. This dose is equivalent to consuming approximately 2 drinks over 1 hour. Administered over a total of 80 minutes.

Active THC and Active EthanolPlacebo THC and Active Ethanol

Control: small amount of alcohol (quarter teaspoon), with no THC. Administered over 20 minutes.

Placebo THC and Active EthanolPlacebo THC and Placebo Ethanol

Eligibility Criteria

Age21 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Males or females 21 to 55 years of age (extremes included).
  • Exposed to cannabis at least once.
  • Exposed to alcohol at least once.
  • Able to provide informed consent.

You may not qualify if:

  • Cannabis naive.
  • Alcohol naive.
  • Positive pregnancy screen
  • Hearing deficits.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Biological Studies Unit, VA Connecticut Healthcare System

West Haven, Connecticut, 06516, United States

Location

MeSH Terms

Conditions

Marijuana Abuse

Condition Hierarchy (Ancestors)

Substance-Related DisordersChemically-Induced DisordersMental Disorders

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Psychiatry

Study Record Dates

First Submitted

March 26, 2015

First Posted

March 31, 2015

Study Start

December 1, 2015

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

April 29, 2026

Record last verified: 2026-04

Locations