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| Sponsor: | National Institute on Drug Abuse (NIDA) |
|---|---|
| Collaborator: |
New York MDRU |
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00015301 |
Purpose
The purpose of this study is to evaluate PET methodology to study in vivo synaptic dopamine release.
| Condition | Intervention | Phase |
|---|---|---|
|
Cocaine-Related Disorders Substance-Related Disorders |
Drug: Methylphenidate |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Diagnostic, Double-Blind, Placebo Control |
| Official Title: | Methylphenidate Raclopride PET Test |
Eligibility| Ages Eligible for Study: | 18 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Healthy normals
Exclusion Criteria:
History of head trauma or loss of consciousness. Significant medical history. History of seizures.
Contacts and Locations
More Information
| Study ID Numbers: | NIDA-5-0013-11, Y01-5-0013-11 |
| Study First Received: | April 18, 2001 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00015301 History of Changes |
| Health Authority: | United States: Federal Government |
|
Cocaine-Related Disorders Dopamine Uptake Inhibitors Neurotransmitter Uptake Inhibitors Neurotransmitter Agents Tranquilizing Agents Disease Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Psychotropic Drugs Central Nervous System Depressants Disorders of Environmental Origin Methylphenidate |
Dopamine Antagonists Central Nervous System Stimulants Antipsychotic Agents Pharmacologic Actions Pathologic Processes Mental Disorders Therapeutic Uses Raclopride Substance-Related Disorders Dopamine Agents Central Nervous System Agents |