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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01853020
Other study ID # 1211011055
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date December 2012
Est. completion date April 7, 2015

Study information

Verified date January 2022
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to characterize the dose-related effects of delta-9-tetrahydrocannabinol (∆9-THC) in healthy individuals on cerebellum-dependent motor functions.


Description:

The overall aim of the current proposal is to investigate whether acute, IV ∆9-THC administration mediates cerebellar versus forebrain-dependent associative learning in humans as assessed with eyeblink conditioning (EBC). In addition, a battery of motor function tests will also be administered (the CANTAB motor screening test, Grooved Pegboard Motor Task, paced finger tapping).


Recruitment information / eligibility

Status Completed
Enrollment 57
Est. completion date April 7, 2015
Est. primary completion date April 7, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 35 Years
Eligibility Inclusion Criteria: - Must have used cannabis at least once in their lifetime - No cannabis use in the past month - Men and women aged 21 to 35 years (extremes included) on the day of the first dosing Exclusion Criteria: - Hearing deficits - Psychiatric or mental disorders - Hearing Deficits

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
THC
Very low dose (0.0015 mg/kg = 0.21 mg in a 70 kg individual) THC, dissolved in alcohol. Administered intravenously over 10 minutes. 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 ¼ of a marijuana cigarette, or "joint". Administered intravenously over 10 minutes. Medium dose (0.03 mg/kg = 2.1 mg in a 70 kg individual) THC, dissolved in alcohol. This dose is roughly equivalent to smoking approximately ½ of a marijuana cigarette, or "joint". Administered intravenously over 10 minutes.
Placebo
Control: small amount of alcohol intravenous (quarter teaspoon), with no THC over 10 minutes.

Locations

Country Name City State
United States VA Connecticut Healthcare System West Haven Connecticut

Sponsors (1)

Lead Sponsor Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cerebellum Dependent Associative Learning (% CRs) % conditioned responses (CRs) will be measured Measured +15 minutes after infusion
Primary Cerebellum Dependent Associative Learning (CR Latency) conditioned response (CR) Latency will be measured Measured +15 minutes after infusion
Primary Completion of the Grooved Pegboard Motor Task (Reaction Time/Accuracy) Total time taken to complete the grooved pegboard tasks will be the dependent measure. Measured +45 minutes after infusion
Primary CANTAB Motor Screening Test (Reaction Time) Using a touch screen, reaction time to touch a target will be the dependent measures. Measured +45 minutes after infusion
Primary CANTAB Motor Screening Test (Accuracy) Using a touch screen, accuracy to touch a target will be the dependent measures. Measured +45 minutes after infusion
Primary Paced Finger Tapping (Correct Responses) Using a button on a computer keyboard, correct responses will be measured. Measured +45 minutes after infusion
Primary Paced Finger Tapping (Reaction Time) Using a button on a computer keyboard, reaction time and tapping variability will be measured. Measured +45 minutes after infusion
Secondary THC intoxication, as measured by the Visual Analog Scale (Total Score) 0 being none; 100 being completely Baseline; +45, +100, +240 minutes after infusion
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