Imaging the Neurochemistry of Drug Addiction With PET

Sponsor
Yale University (Other)
Overall Status
Recruiting
CT.gov ID
NCT02817698
Collaborator
National Institute on Drug Abuse (NIDA) (NIH)
90
3
1
57.1
30
0.5

Study Details

Study Description

Brief Summary

The investigators' project has two overarching goals. 1) The investigators will use newly developed positron emission tomography (PET) technology to investigate the dopaminergic neurochemistry of drugs of abuse including marijuana, traditional cigarettes, and cocaine, and 2) The investigators will extend PET technology to an additional neurotransmitter system

  • namely, the opioid-ergic system, using the same drugs of abuse.
Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

Aim 1. To examine the magnitude, location and timing of drug-induced dopamine release.

  1. Tobacco smokers (n=20) will be imaged with [11C]raclopride PET, after overnight abstinence from tobacco. Subjects will smoke their preferred brand of cigarette during the PET scan.

  2. Marijuana smokers (n=20) will be imaged with [11C]raclopride PET, after overnight abstinence from marijuana. Subjects will smoke a marijuana cigarette during the PET scan.

  3. Cocaine users (n=20) will be imaged with [11C]raclopride PET, after overnight abstinence from cocaine. Subjects will be administered cocaine during the PET scan.

Aim 2. To examine the magnitude, location and timing of drug-induced beta-endorphin release. *The Investigators will attempt to use the same subjects from Aim 1 for Aim 2.

  1. Tobacco smokers (n=20) will be imaged with [11C]carfentanil PET, after overnight abstinence from tobacco. Subjects will smoke their preferred brand of cigarette during the PET scan.

  2. Marijuana smokers (n=20) will be imaged with [11C]carfentanil PET, after overnight abstinence from marijuana. Subjects will smoke a marijuana cigarette during the PET scan.

  3. Cocaine users (n=20) will be imaged with [11C]carfentanil PET, after overnight abstinence from cocaine. Subjects will be administered cocaine during the PET scan.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Imaging the Neurochemistry of Drug Addiction With PET
Actual Study Start Date :
Nov 29, 2017
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Drug of dependence

There is only one arm to the study. All subjects will receive their drug of dependence in this study. Nicotine dependent subjects will receive tobacco cigarettes, cannabis dependent subjects will receive cannabis cigarettes, and cocaine dependent subjects will receive IV cocaine.

Drug: cannabis
All cannabis dependent subjects will use cannabis cigarettes to induce elevated dopamine and beta endorphin levels in the brain.
Other Names:
  • marijuana
  • Outcome Measures

    Primary Outcome Measures

    1. Change in dopamine levels at baseline and after drug of dependence administration as confirmed by PET images. [90 minute PET scan acquisition. Drug of dependence will be given at -35 mins]

      PET images will be obtained in dependent subjects at baseline and after drug of dependence administration. Change in DA levels will be determined by change in binding potential of raclopride.

    2. Change in beta endorphin levels at baseline and after drug of dependence administration as confirmed by PET images. [120 minute PET scan acquisition. Drug of dependence will be given at -35 mins]

      PET images will be obtained in dependent subjects at baseline and after drug of dependence administration. Change in beta endorphin levels will be determined by change in binding potential of carfentanil.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 55 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • General Inclusion Criteria:
    1. Men and women, aged 18-55 years

    2. Able to read and write English and give voluntary written informed consent

    3. Not treatment seeking or using treatment medications

    Tobacco Smokers

    1. Have a Fagerström Test for Nicotine Dependence (FTND) rating of at least 3.

    2. Have been using at least 7 cigarettes per day for at least 1 year

    3. Carbon monoxide levels > 10 ppm during intake evaluation

    4. Urine cotinine levels of > 150 ng/mL during intake evaluation

    5. Are not current users of marijuana or other illicit drugs

    Marijuana Smokers

    1. Meet DSM-V criteria for cannabis use disorder based on the structured clinical interview diagnostic (SCID) or regular cannabis use of >5 times/week

    2. Test positive for THC

    3. Have been smoking cannabis on a regular basis for > 1 year

    Cocaine Users

    1. DSM-V criteria for Cocaine Abuse or Dependence

    2. Recent street cocaine use in excess of amounts to be administered in the current study

    3. Intravenous and/or smoked (crack/ freebase) use

    4. Positive urine toxicology screen for cocaine

    Exclusion Criteria:
      1. Current significant medical condition such as neurological, cardiovascular, endocrine, renal, liver, or thyroid pathology.
    1. History of or current neurological or significant psychiatric disorder such as schizophrenia or bipolar disorder (DSM-IV Axis 1).

    2. History of significant head trauma. 4. Women who are pregnant or nursing, or fail to use one of the following methods of birth control unless she or partner is surgically sterile or she is postmenopausal (hormone contraceptives [oral, implant, injection, patch, or ring], contraceptive sponge, double barrier [diaphragm or condom plus spermicide], or IUD).

    3. Regular or current significant use of any prescription, herbal or illegal psychotropic medications (e.g., antidepressants, antipsychotics, anxiolytics, ecstasy) in the past 6 mo, with no current illegal drug use confirmed by urine toxicology (except for cocaine and marijuana when relevant).

    4. Significant substance misuse (including alcohol, and excluding cannabis and marijuana when relevant) that in the PI's determination interferes with the study results or safety of the subject.

    5. Have MRI-incompatible implants and other contraindications for MRI, such as a pacemaker, artificial joints, non-removable body piercings, claustrophobia, etc.

    6. Subjects with history of prior radiation exposure for research purposes within the past year such that participation in this study would place them over FDA limits for annual radiation exposure. This guideline is an effective dose of 5 rem received per year.

    7. Subjects with current, past or anticipated exposure to radiation in the work place within one year of proposed research PET scans.

    8. Subjects with history of IV drug use which would prevent venous access for PET tracer injection.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Connecticut Mental Health Center New Haven Connecticut United States 06519
    2 Yale Magnetic Resonance Research Center New Haven Connecticut United States 06519
    3 Yale PET Center New Haven Connecticut United States 06519

    Sponsors and Collaborators

    • Yale University
    • National Institute on Drug Abuse (NIDA)

    Investigators

    • Principal Investigator: Kelly Cosgrove, PhD, Yale University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kelly Cosgrove, Associate Professor, Yale University
    ClinicalTrials.gov Identifier:
    NCT02817698
    Other Study ID Numbers:
    • 1604017594
    • 1R01DA038709-01A1
    • 1R01DA038832-01A1
    • 1R03DA047588-01
    First Posted:
    Jun 29, 2016
    Last Update Posted:
    May 4, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Kelly Cosgrove, Associate Professor, Yale University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 4, 2022