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Completed

NCT Number: NCT01790490

Glutamatergic Modulation of Cocaine-related Deficits

Cocaine dependence involves problematic neuroadaptations, such as heightened reactivity to cocaine cues, that may be responsive to pharmacological modulation of glutamatergic circuits. Despite promising preclinical findings with n-methyl-d-aspartate receptor (NMDAr) modulators, studies with human subjects have been unsuccessful to date. The purpose of this investigation is to examine the effects of the NMDAr antagonist ketamine, recently found to have potent therapeutic effects in humans, on cue-induced craving and impaired motivation for quitting cocaine in cocaine dependent participants, 24-hours post-infusion.

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Key information

Age range

21 year–52 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

NYSPI

New York, 10032, United States

About this study

In this study, volunteers will undergo a 9 day inpatient trial during which they will receive three counter-balanced infusions (two doses of ketamine and a dose of lorazepam) on three separate days in a within-subject, double-blind, controlled design. Of the various glutamate antagonists available for human use, ketamine will be utilized because its safety profile, pharmacokinetics, and range of tolerable sub-anesthetic dosings have been very well studied. Also, ketamine has shown promise in managing opiate and alcohol use disorders in certain studies, and may therefore be the most likely glutamate antagonist to dampen cue reactivity and increase motivation in cocaine users. If ketamine significantly improves these deficits, this would suggest that the drug should be investigated further for potential utility as a treatment for cocaine dependence.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Active free-base cocaine dependence (at least 4 days of use over the past month, with at least 1 use per week); if the participant uses through another route (IN, IV), then the FB route is dominant (> 80% of occasions).
  • Physically healthy
  • No adverse reactions to study medications
  • 21-52 years of age
  • Normal body weight
  • Responsive to drug cues
  • Capacity to consent

Exclusion criteria

  • Seeking treatment or abstinence
  • DSM IV criteria for substance dependence (other than methamphetamine, cocaine, cannabis, or nicotine), or DSM IV criteria for abuse of ketamine or lorazepam
  • DSM-IV criteria for other Axis I psychiatric illness that may make participation hazardous such as schizophrenia, schizoaffective disorder, psychosis NOS, MDD, psychosis secondary to substances, or bipolar disorder
  • Delirium, Dementia, Amnesia, Cognitive Disorders, or dissociative disorders
  • Current suicide risk or a history of suicide attempt within the past 2 years
  • Current use of prescribed psychotropic medication
  • Pregnancy, nursing, or had a baby within the past 6 mo.
  • Heart disease as indicated by history, abnormal ECG, previous cardiac surgery.
  • Unstable physical disorders which might make participation hazardous such as end-stage AIDS, hypertension (>140/90), anemia, active hepatitis or other liver disease, or diabetes
  • "Bad" reaction/experience with prior exposure to ketamine or lorazepam
  • History of significant violence
  • First degree relative with a psychotic disorder

Treatment and study plan

Ketamine 0.41 mg/kg

Drug

52 minute iv infusion of ketamine 0.41 mg/kg

Other names: K1

Ketamine 0.71 mg/kg

Drug

52 minute iv infusion of ketamine 0.71 mg/kg. This dose follows K1 in all 3 orderings.

Other names: K2

Lorazepam 2 mg

Drug

52 minute infusion of lorazepam 2 mg. This serves as an active control.

Other names: LZP

Primary outcomes

  1. Change in Cue Reactivity

    Time frame: Baseline and 24 hours after infusion

    Serial visual analogue scale (VAS) scores for craving elicited by cocaine cue: units on a scale (0-200), high is worse. Scores are obtained at baseline and at 24 hours after the infusion.

  2. Change in Motivation to Quit

    Time frame: Baseline and 24 hours post-infusion

    Motivation score obtained from the University of Rhode Island Change Assessment (URICA). Scores are obtained at baseline and at 24 hours after each infusion. The scores are 0-13, with higher scores indicating greater motivation. The analysis is within-subject. Scores included below are means; higher scores represent higher motivation to quit than do lower scores.

Sponsors and collaborators

Lead sponsor

New York State Psychiatric Institute

Other

Registry information

Official study title

The Effect of Ketamine on Reducing Cue Reactivity in Cocaine Users

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Feb 13, 2013
Registry last updated
Apr 30, 2019

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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