Skip to content

Glutamatergic Modulation of Motivation Enhancement: A Pilot Feasibility Trial

Glutamatergic Modulation of Motivation Enhancement: A Pilot Feasibility Trial

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02373124
Enrollment
4
Registered
2015-02-26
Start date
2014-12-31
Completion date
2016-10-31
Last updated
2020-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cocaine Use Disorders

Brief 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.

Interventions

DRUGinfusion of NMDA antagonist

52 minute infusion

Sponsors

New York State Psychiatric Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

Inclusion Criterion Method of Ascertainment 1. 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 2. Physically healthy Laboratory tests (urinalysis, blood chemistry, 12-lead ECG in normal limits), physical examination, self-reported medical history 3. No adverse reactions to study medications Subjects will be asked about previous exposure to ketamine and midazolam 4. 21-55 years of age Self-reported age, verification with legal identification 5. Capacity to consent and comply with study procedures, including sufficient proficiency in English A short written test about study procedures, SCID, psychiatric interview 6. Seeking treatment Psychiatric Interview, self-report Exclusion Criterion Method of Ascertainment 1. 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 2. Physiological dependence on another substance, such as alcohol, opioids, or benzodiazepines, excluding caffeine, nicotine, and cannabis SCID, Psychiatric Interview 3. Delirium, Dementia, Amnesia, Cognitive Disorders, or Dissociative disorders SCID, Psychiatric Interview 4. Current suicide risk or a history of suicide attempt within the past year SCID, Psychiatric Interview 5. Pregnant or interested in becoming pregnant during the study period Blood and urine pregnancy testing, self-report 6. 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 7. Unstable physical disorders which might make participation hazardous such as end-stage AIDS, hypertension (\>140/90), WBC \< 3.5, active hepatitis or other liver disease with elevated transaminase levels (\< 2-3 X upper limit of normal will be considered acceptable if PT/PTT is normal), renal failure (creat \> 2, BUN \>40), or untreated diabetes Physiological tests (urinalysis, blood chemistry, 12-lead ECG), physical examination, self-reported medical history 8. 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 9. Recent history of significant violence (past 2 years) SCID, Psychiatric Interview 10. Abnormal pseudocholinesterase level Blood testing 11. First degree relative with a psychotic disorder (bipolar disorder, schizophrenia, schizoaffective disorder, or psychosis NOS) SCID, Psychiatric Interview 12. BMI \> 35, or a history of documented obstructive sleep apnea Physical examination, self-reported medical history 13. On psychotropic or other medications whose effect could be disrupted by participation in the study Psychiatric interview, self-reported medical history 14. Patients who cannot comply with study procedures during the initial hospitalization phase Study Performance

Design outcomes

Primary

MeasureTime frameDescription
Cocaine Use5 weeksParticipants were provided choices to use up to 5 hits of cocaine on up to 2 occasions (cocaine versus money). Participants who chose cocaine (1 or more hits) during the first choice opportunity are administered a 52 minute infusion of 0.71 mg/kg ketamine the following day. Another choice opportunity occurs 24 hours later. The primary outcome is the choice participants made during these occasions

Countries

United States

Participant flow

Participants by arm

ArmCount
Open-label
52 minute infusion of NMDA antagonist infusion of NMDA antagonist: 52 minute infusion
4
Total4

Baseline characteristics

CharacteristicOpen-label
Age, Continuous50.5 years
Sex: Female, Male
Female
1 Participants
Sex: Female, Male
Male
3 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 4
other
Total, other adverse events
0 / 4
serious
Total, serious adverse events
0 / 4

Outcome results

Primary

Cocaine Use

Participants were provided choices to use up to 5 hits of cocaine on up to 2 occasions (cocaine versus money). Participants who chose cocaine (1 or more hits) during the first choice opportunity are administered a 52 minute infusion of 0.71 mg/kg ketamine the following day. Another choice opportunity occurs 24 hours later. The primary outcome is the choice participants made during these occasions

Time frame: 5 weeks

Population: medically healthy, treatment-seeking cocaine dependent individuals without a history of abuse of or adverse reaction to ketamine or benzodiazepines.

ArmMeasureGroupCategoryValue (COUNT_OF_PARTICIPANTS)
Open-labelCocaine Usefirst choice opportunityable to abstain3 Participants
Open-labelCocaine Usefirst choice opportunitycontinue to use1 Participants
Open-labelCocaine Usesecond choice opportunityable to abstain1 Participants
Open-labelCocaine Usesecond choice opportunitycontinue to use0 Participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026