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Phase 2 N=4 Treatment

Glutamatergic Modulation of Motivation Enhancement: A Pilot Feasibility Trial

Cocaine Use Disorders

Enrolled (actual)
4
Serious AEs
0.0%
Results posted
Apr 2019
Primary outcome: Primary: Cocaine Use — 3; 1; 1; 0 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
infusion of NMDA antagonist (Drug)
Age
Adult · 21+ yrs
Sex
All
Sponsor
New York State Psychiatric Institute
Primary completion
Oct 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Cocaine Use
3; 1; 1; 0

Summary

This study evaluates the feasibility of a treatment paradigm that involves naturalistic cocaine use opportunities in the context of psychotherapy aimed at utilizing these opportunities therapeutically.

Eligibility Criteria

Inclusion Criterion Method of Ascertainment

  • Active cocaine dependence with at least 8 days of use or at least 4 binges of large amounts (>$200/occasion) over the past 30 days, and displaying at least one positive utox during screening SCID, Psychiatric Interview, self-report, utox
  • Physically healthy Laboratory tests (urinalysis, blood chemistry, 12-lead ECG in normal limits), physical examination, self-reported medical history
  • No adverse reactions to study medications Subjects will be asked about previous exposure to ketamine and midazolam
  • 21-55 years of age Self-reported age, verification with legal identification
  • Capacity to consent and comply with study procedures, including sufficient proficiency in English A short written test about study procedures, SCID, psychiatric interview
  • Seeking treatment Psychiatric Interview, self-report

Exclusion Criterion Method of Ascertainment

  • Meets DSM IV criteria for current major depression, bipolar disorder, schizophrenia, any psychotic illness, including substance induced psychosis, and current substance-induced mood disorder with HAMD score > 12. Psychiatric Interview, SCID, HAMD
  • Physiological dependence on another substance, such as alcohol, opioids, or benzodiazepines, excluding caffeine, nicotine, and cannabis SCID, Psychiatric Interview
  • Delirium, Dementia, Amnesia, Cognitive Disorders, or Dissociative disorders SCID, Psychiatric Interview
  • Current suicide risk or a history of suicide attempt within the past year SCID, Psychiatric Interview
  • Pregnant or interested in becoming pregnant during the study period Blood and urine pregnancy testing, self-report
  • Any of the following cardiac conditions: clinically significant left ventricular hypertrophy, angina, clinically significant arrhythmia, or mitral valve prolapse Laboratory tests (12-lead ECG in normal limits), physical examination, self-reported medical history
  • Unstable physical disorders which might make participation hazardous such as end-stage AIDS, hypertension (>140/90), WBC 2, BUN >40), or untreated diabetes Physiological tests (urinalysis, blood chemistry, 12-lead ECG), physical examination, self-reported medical history
  • Previous history of ketamine or midazolam misuse or abuse, and a history of an adverse reaction/experience with prior exposure to cocaine, ketamine or midazolam Physical examination, self-reported medical history
  • Recent history of significant violence (past 2 years) SCID, Psychiatric Interview
  • Abnormal pseudocholinesterase level Blood testing
  • First degree relative with a psychotic disorder (bipolar disorder, schizophrenia, schizoaffective disorder, or psychosis NOS) SCID, Psychiatric Interview
  • BMI > 35, or a history of documented obstructive sleep apnea Physical examination, self-reported medical history
  • On psychotropic or other medications whose effect could be disrupted by participation in the study Psychiatric interview, self-reported medical history
  • Patients who cannot comply with study procedures during the initial hospitalization phase Study Performance
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02373124). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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