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Completed

NCT Number: NCT02181491

PET Imaging in Cocaine Self Administration

There has been recent interest in the role of the 5-HT1B receptor as a possible modulating factor in cocaine dependence, certainly in preclinical models. The Yale Positron Emission Tomography (PET) Center has developed a novel 5-HT1B receptor antagonist radioligand, [11C]-P943, which has been validated in human studies. We hypothesize that the 5-HT1B receptor plays a key role in cocaine dependence. The long term goal of this project would be to study pharmacological manipulation of the 5-HT1B receptor as a potential molecular target for cocaine dependence.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Connecticut Mental Health Center

New Haven, Connecticut, 06519, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • age 18 - 50 years
  • voluntary, written, informed consent
  • physically healthy by medical history, physical, neurological, ECG, and laboratory examinations
  • for females, non-lactating, no longer of child-bearing potential (or agree to practice effective contraception during the study), and a negative serum pregnancy (B-HCG) test
  • English speaking
  • No other major Axis DSM-IV diagnosis present, besides required as below

Inclusion criteria

for cocaine dependent:

  • DSM-IV criteria for Cocaine Abuse (305.60) or Cocaine Dependence (304.20)
  • recent street cocaine use
  • intravenous and/or smoked (crack/ freebase) use
  • positive urine toxicology screen for cocaine

Inclusion criteria

for healthy controls:

  • No current, or history of, any DSM-IV diagnosis
  • No first-degree relative with history of psychotic, mood, or anxiety disorder

Exclusion criteria

  • medical contraindications to AMPT administration (e.g., known sensitivity/reaction to AMPT)
  • medical contraindications to MPH administration (e.g., history of cardiac problems, seizures, etc.)
  • drug or alcohol dependence (except nicotine)
  • a primary major DSM-IV psychiatric diagnosis (schizophrenia, bipolar disorder, etc.), unrelated to cocaine or pathological gambling
  • positive answers on the cardiac screening questionnaire that may place the subject at higher risk, as determined by cardiologist review of both the questionnaire responses and screening ECG
  • current use of psychotropic and/or potentially psychoactive prescription medication
  • physical or laboratory (B-HCG) evidence of pregnancy
  • clotting disorders or recent anticoagulant therapy
  • MRI-incompatible implants and other contraindications for MRI (i.e., aneurysm clip, metal fragments, internal electrical devices such as a cochlear implant, spinal cord stimulator or pacemaker)
  • history of claustrophobia or feeling of inability to lie still on his back for the PET or MRI scans
  • history of prior radiation exposure for research purposes within the past year such that participation in this study would place them over Radioactive Drug Research Committee (RDRC) limits for annual radiation exposure. This guideline is an effective dose of 5 rem received per year
  • donation or loss of 550 mL of blood or more (including plasmapheresis) or receipt of a transfusion of any blood product within 8 weeks prior to the first dose of study drug
  • use any prescription medications and/or over-the-counter medications, vitamins and/or herbal supplements within 2 weeks prior to study and for the duration of the study without approval from the study doctor
  • eat grapefruit or grapefruit products, and drink alcohol, and anything containing caffeine 3 days before study and during study
  • For CD subjects, < 1 year of cocaine dependence
  • Subjects with current, past, or anticipated exposure to radiation in the workplace

Treatment and study plan

[11C]-P943

Other

Primary outcomes

  1. BPND

    Time frame: 1 week

    BPND is a measure of serotonin receptor availability

Sponsors and collaborators

Lead sponsor

Yale University

Other

Registry information

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Jul 4, 2014
Registry last updated
Nov 19, 2020

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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