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Assessment of Interactions Between Methamphetamine and Aripiprazole - 1
This study is ongoing, but not recruiting participants.
Sponsored by: National Institute on Drug Abuse (NIDA)
Information provided by: National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier: NCT00089440
  Purpose

The purpose of this study is to assess the interactions between intravenous methamphetamine and aripiprazole.


Condition Intervention Phase
Amphetamine-Related Disorders
Drug: Aripiprazole
Phase I

MedlinePlus related topics: Methamphetamine
Drug Information available for: Aripiprazole Amphetamine Methamphetamine
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Placebo Control
Official Title: Assessment of Interactions Between IV Methamphetamine and Aripiprazole

Further study details as provided by National Institute on Drug Abuse (NIDA):

Primary Outcome Measures:
  • Adverse effect measures
  • pharmacokinetic assessment

Estimated Enrollment: 17
Study Start Date: June 2004
Estimated Study Completion Date: March 2005
Detailed Description:

This is a double-blind, placebo-controlled human laboratory clinical pharmacology study to assess potential interactions between intravenous d-methamphetamine infusion and treatment with oral aripiprazole.

  Eligibility

Ages Eligible for Study:   18 Years to 45 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Must meet DSM-4 criteria for methamphetamine abuse or dependence and are non-treatment seeking.
  • Ability to verbalize understanding of the consent form, able to provide written informed consent, and verbalize willingness to complete study procedures.

Exclusion Criteria:

  • Please contact the site for more information.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00089440

Locations
United States, California
UCLA Integrated Substance Abuse Program
Los Angeles, California, United States, 90024
United States, New York
New York University, School of Medicine
New York, New York, United States, 10016
Sponsors and Collaborators
Investigators
Principal Investigator: Thomas Newton, M.D. University of California, Los Angeles
  More Information

Study ID Numbers: NIDA-MDS-0002-1
Study First Received: August 5, 2004
Last Updated: October 25, 2007
ClinicalTrials.gov Identifier: NCT00089440  
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Methamphetamine
Dopamine
Mental Disorders
Amphetamine-Related Disorders
Substance-Related Disorders
Disorders of Environmental Origin
Amphetamine
Aripiprazole

Additional relevant MeSH terms:
Dopamine Uptake Inhibitors
Neurotransmitter Uptake Inhibitors
Neurotransmitter Agents
Tranquilizing Agents
Molecular Mechanisms of Pharmacological Action
Adrenergic Agents
Sympathomimetics
Adrenergic Uptake Inhibitors
Physiological Effects of Drugs
Psychotropic Drugs
Central Nervous System Depressants
Central Nervous System Stimulants
Antipsychotic Agents
Pharmacologic Actions
Autonomic Agents
Therapeutic Uses
Dopamine Agents
Peripheral Nervous System Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on January 14, 2009