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Cocaethylene as a Treatment for Cocaine Dependence - 1

Primary Purpose

Cocaine-Related Disorders

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Cocaethylene
Sponsored by
National Institute on Drug Abuse (NIDA)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cocaine-Related Disorders focused on measuring cocaine dependence

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Meets DSM-IV criteria for cocaine dependence Cocaine use of at least 0.5 grams each week during the three months prior to enrollment, confirmed by a positive urine test for cocaine metabolite Females are eligible if currently using adequate contraception, not planning to become pregnant, or surgically sterilized Females of child-bearing potential must have a negative pregnancy test prior to study entry Currently not physiologically dependent on alcohol, but may meet DSM-IV criteria for alcohol abuse or dependence Exclusion Criteria: Meets DSM-IV criteria for dependence on any drugs (other than nicotine or alcohol) within the year prior to enrollment Currently abuses other substances such as opiates, sedative-hypnotics, or amphetamines (excluding marijuana or nicotine) more than twice a week History of a serious medical illness or indication of a serious medical illness such as seizures, hypertension, heart disease, an abnormal ECG, anemia, diabetes, or abnormal blood flow sounds Meets DSM-IV criteria for a current major mental disorder, including major depression, bipolar disorder, schizophrenia, schizophreniform disorder, schizoaffective disorder, mental retardation, or organic mental syndrome Currently being treated with psychotropic medication At risk for suicide, as determined by a psychiatrist Greater than two times the normal level for liver or kidney function tests Currently seeking treatment for drug abuse Participants with liver function tests equal to or greater than three times the normal level will be discontinued from the study

Sites / Locations

  • Virginia Commonwealth University

Outcomes

Primary Outcome Measures

Clinical physiological response to cocaine challenge - especially adverse effects measures

Secondary Outcome Measures

Full Information

First Posted
July 22, 2005
Last Updated
January 11, 2017
Sponsor
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00124696
Brief Title
Cocaethylene as a Treatment for Cocaine Dependence - 1
Official Title
Cocaethylene Substitution Therapy and Tolerance Induction in Treating Cocaine Dependence
Study Type
Interventional

2. Study Status

Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
December 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute on Drug Abuse (NIDA)

4. Oversight

5. Study Description

Brief Summary
Cocaine has been cited as the primary drug threat in the United States. The purpose of this study is to determine if cocaethylene, used as a prototype drug, is a safe and effective treatment for cocaine dependence.
Detailed Description
Currently, there are no medications available to specifically treat cocaine addiction. Cocaethylene is an active metabolite of cocaine and has a similar chemical structure to cocaine. The purpose of this study is to determine whether substitution therapy with cocaethylene is a safe and effective treatment for cocaine dependence. This double-blind, placebo-controlled trial will occur in 3 parts. In Part 1, the individual pharmacokinetics of an intravenous dose of cocaethylene will be determined in order to estimate individualized cocaethylene infusion rates and pharmacokinetic parameters. This will provide important information on how cocaethylene is processed by the body. In Part 2, an infusion of cocaethylene, producing a venous plasma concentration of 200 ng/ml, will be administered over an 8-hour period. Clinical monitoring and blood sampling will occur in order to determine the safety profile of cocaethylene. During Part 3, the ability of cocaethylene to modify the acute effects of intravenous cocaine will be determined. Cocaethylene will be administered in plasma concentrations of 0 ng/ml, 50 ng/ml, or 200 ng/ml over an 8-hour period. Participants will be randomly assigned to receive a challenge intravenous dose of cocaine (0.5 mg/kg or 1 mg/kg) or placebo at the 4-hour mark of cocaethylene infusion. Following the initial 8-hour period, cocaethylene infusion will be continued for an additional 5 hours. Behavioral and physiological measures will be collected throughout the study sessions at predetermined times to evaluate whether tolerance to cocaethylene develops. These measures will also help to determine whether cocaethylene modifies or produces tolerance to the effects of an acute dose of cocaine.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine-Related Disorders
Keywords
cocaine dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
8 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Cocaethylene
Primary Outcome Measure Information:
Title
Clinical physiological response to cocaine challenge - especially adverse effects measures

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meets DSM-IV criteria for cocaine dependence Cocaine use of at least 0.5 grams each week during the three months prior to enrollment, confirmed by a positive urine test for cocaine metabolite Females are eligible if currently using adequate contraception, not planning to become pregnant, or surgically sterilized Females of child-bearing potential must have a negative pregnancy test prior to study entry Currently not physiologically dependent on alcohol, but may meet DSM-IV criteria for alcohol abuse or dependence Exclusion Criteria: Meets DSM-IV criteria for dependence on any drugs (other than nicotine or alcohol) within the year prior to enrollment Currently abuses other substances such as opiates, sedative-hypnotics, or amphetamines (excluding marijuana or nicotine) more than twice a week History of a serious medical illness or indication of a serious medical illness such as seizures, hypertension, heart disease, an abnormal ECG, anemia, diabetes, or abnormal blood flow sounds Meets DSM-IV criteria for a current major mental disorder, including major depression, bipolar disorder, schizophrenia, schizophreniform disorder, schizoaffective disorder, mental retardation, or organic mental syndrome Currently being treated with psychotropic medication At risk for suicide, as determined by a psychiatrist Greater than two times the normal level for liver or kidney function tests Currently seeking treatment for drug abuse Participants with liver function tests equal to or greater than three times the normal level will be discontinued from the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elinore Mccance-Katz, M.D., Ph.D.
Organizational Affiliation
Yale Psychiatric Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Virginia Commonwealth University
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23298
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Cocaethylene as a Treatment for Cocaine Dependence - 1

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