Assessment of the Potential Interactions Between Cocaine and GBR 12909 - 1
The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2005 by National Institute on Drug Abuse (NIDA).
Recruitment status was Active, not recruiting
Recruitment status was Active, not recruiting
Sponsor:
Information provided by:
National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier:
NCT00051896
First received: January 17, 2003
Last updated: April 25, 2012
Last verified: March 2005
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Purpose
The purpose of this study is to assess the potential interactions between iv cocaine and GBR 12909.
| Condition | Intervention | Phase |
|---|---|---|
|
Cocaine-Related Disorders |
Drug: GBR 12909 |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Double-Blind, Placebo-Controlled, Dose Escalating, Safety and Pharmacology Study With Three Dosages of GBR 12909 in Cocaine Experienced Volunteers |
Resource links provided by NLM:
Further study details as provided by National Institute on Drug Abuse (NIDA):
Primary Outcome Measures:
- Pharmacokinetic parameter comparison
| Estimated Enrollment: | 24 |
| Study Start Date: | August 2002 |
This is a single dose with escalation, double-blind, placebo-controlled inpatient study in which 24 cocaine experienced volunteers that meet protocol eligibility criteria during a 30 day screen period will be randomized into three dose groups.
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Must understand study procedures and provide written informed consent
- For additional inclusion criteria information, please contact study site for more information.
Exclusion Criteria:
- Please contact study site for more information.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00051896
Locations
| United States, Maryland | |
| Uniformed Services University of Health Science | |
| Bethesda, Maryland, United States, 20814 4799 | |
Sponsors and Collaborators
Investigators
| Principal Investigator: | Louis Cantilena, M.D. | Uniformed Services University of Health Science |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00051896 History of Changes |
| Other Study ID Numbers: | NIDA-CPU-0002-1 |
| Study First Received: | January 17, 2003 |
| Last Updated: | April 25, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Cocaine-Related Disorders Substance-Related Disorders Mental Disorders Vanoxerine Dopamine Uptake Inhibitors Dopamine Agents |
Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Neurotransmitter Uptake Inhibitors Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 19, 2013