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Completed

NCT Number: NCT01638364

Dopamine Release in the Human Brain Following Alcohol Administration

The purpose of this study is to examine whether there is an increase in dopamine levels in the human striatum following an oral administration of alcohol, as has been evidenced in animal models. This will be a Positron Emission Tomography (PET) study using the radiotracer, [11C]-(+)-PHNO (11C]-( + )-4-propyl- 3,4,4a,5,6,10b-hexahydro-2H-naphtho[1,2-b][1,4]oxazin-9-ol).

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Key information

Conditions

Age range

21 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Centre for Addiction and Mental Health

Toronto, Ontario, M5T 1R8, Canada

About this study

This will be a within subjects study in 8 heavy drinkers ages 21-45. The within factors will be PET scans following an alcoholic beverage and following a non-alcoholic beverage. Participants will also have a baseline session prior to the scans where they will complete various cognitive tasks and questionnaires. During each PET scan, subjective drug effects as well as heart rate, blood pressure, blood alcohol content and cortisol levels will be collected. The change in PHNO binding potential between the two scan conditions will be the primary outcome measure.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy males and females of any ethnic origin between 21 and 45 years old.
  • Reported consumption of at least two heavy drinking episodes (according to the National Institute on Alcohol Abuse and Alcoholism (NIAAA) criterion of 5 drinks for males or 4 for females) in the past 30 days prior to assessment.
  • Willing and capable to provide written informed consent
  • Good command of the English language

Exclusion criteria

  • Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) diagnosis of alcohol dependence; receiving treatment for alcohol dependence
  • Taking medications or have any medical condition for which alcohol is contraindicated
  • Any medical condition requiring immediate investigation or treatment
  • Previous head trauma/neurological condition such as clinically significant history of seizure disorder, a history of clinically significant head trauma (i.e., concussion resulting in clinically significant loss of consciousness) or past intracranial surgery
  • Beck Depression Inventory score >16
  • Current active or past suicidal ideation
  • Pregnancy tested by urine and blood screen each PET study day or lactation
  • Current DSM-IV diagnosis of any Axis I psychiatric disorder
  • Regular use of any therapeutic or recreational psychoactive drug use during the last three months (with the exception of nicotine and alcohol) or other substance use disorder (including nicotine)
  • Abnormal body mass (as defined as not within 20% of normal body mass index).
  • Current past or anticipated exposure to radiation exceeding 20 mSv in the last year.
  • Metal implants or paramagnetic objects within the body which may interfere with the magnetic resonance imaging (MRI).
  • Claustrophobia or a history of panic attacks
  • Abnormal clinical laboratory findings including serum creatinine greater than 2.0 mg/dl, abnormal liver function tests, elevated serum bilirubin (more than 1.5 times upper limit of normal), or pre-trial electrocardiogram (EKG) results demonstrating clinical significant abnormality

Treatment and study plan

alcoholic beverage

Drug

An appropriate amount of 95% USP ethyl alcohol will be mixed in orange juice and tonic water to obtain a drink equivalent to 3-5 standard drinks. The beverage will be consumed over a period of 15 minutes.

Other names: Ethyl alcohol 95%

non-alcoholic beverage

Drug

This beverage will be a mixture of orange juice and tonic water. The beverage will be consumed over a period of 15 minutes.

Other names: Tropicana orange juice and Schweppes tonic water.

Primary outcomes

  1. Change in PHNO Binding Potential

    Time frame: 2 weeks

    Following the injection of the positron-emitting radiotracer [11C]-(+)-PHNO, binding of this radiotracer to dopamine receptors (DR) D2/3 will be measured using the PET scanner. As dopamine also binds to DR D2/3, either an increase or decrease in dopamine levels will either decrease or increase PHNO occupancy respectively. [11C]-(+)-PHNO binding potential will be measured on two different conditions (alcoholic beverage vs non-alcoholic beverage) on two separate days.

Secondary outcomes

  1. Subjective effects of alcohol

    Time frame: 2 weeks

    During the PET scans, the subjective effects ( Alcohol Urges Scale, Biphasic Alcohol Effects Scale)of alcohol will be assessed at various time points throughout beverage consumption and PET scan.

  2. Objective effects of alcohol

    Time frame: 2 weeks

    During the PET scans, the objective effects of alcohol (blood pressure, heart rate, blood alcohol content, blood cortisol levels) will be assessed at various time points throughout the drink consumption and PET scan.

Sponsors and collaborators

Lead sponsor

Centre for Addiction and Mental Health

Other

Registry information

Official study title

Imaging Alcohol Induced Dopamine Release in the Human Brain: a PET/[11C](+)PHNO Study

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Jul 11, 2012
Registry last updated
Jul 28, 2015

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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