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Predictive Values of Serotonergic Alterations for Outcome - 2
This study has been terminated.
Sponsors and Collaborators: National Institute on Drug Abuse (NIDA)
Department of Veterans Affairs
Information provided by: National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier: NCT00000313
  Purpose

The purpose of this study is to evaluate the predictive value of serotonergic alterations for outcome.


Condition Intervention Phase
Cocaine-Related Disorders
Drug: Fenfluramine
Phase I

Drug Information available for: Fenfluramine Fenfluramine hydrochloride
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment
Official Title: Predictive Values of Serotonergic Alterations for Outcome

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

Primary Outcome Measures:
  • Side effects
  • Neuroendocrine changes
  • Psychological changes
  • Craving

Estimated Enrollment: 0
  Eligibility

Ages Eligible for Study:   25 Years to 50 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Please contact site for information.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00000313

Locations
United States, New York
VA Medical Center
Brooklyn, New York, United States, 11209
Sponsors and Collaborators
Investigators
Principal Investigator: Laure Buydens-Branchey, M.D. Department of Veterans Affairs
  More Information

Study ID Numbers: NIDA-09468-2, R01-09468-2
Study First Received: September 20, 1999
Last Updated: June 23, 2005
ClinicalTrials.gov Identifier: NCT00000313  
Health Authority: United States: Federal Government

Study placed in the following topic categories:
Cocaine-Related Disorders
Mental Disorders
Substance-Related Disorders
Disorders of Environmental Origin
Fenfluramine
Serotonin

Additional relevant MeSH terms:
Neurotransmitter Uptake Inhibitors
Neurotransmitter Agents
Serotonin Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Serotonin Uptake Inhibitors
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 15, 2009