Phase 2
N=4
Glutamatergic Modulation of Motivation Enhancement: A Pilot Feasibility Trial
Cocaine Use Disorders
Bottom Line
View on ClinicalTrials.gov: NCT02373124 ↗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
| Outcome | Result | p-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
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.