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Neurobiology of Opioid Dependence: 2 - 2
This study has been completed.
Sponsors and Collaborators: National Institute on Drug Abuse (NIDA)
Yale University
Information provided by: National Institute on Drug Abuse (NIDA)
ClinicalTrials.gov Identifier: NCT00000193
  Purpose

The purpose of this study is to evaluate the effects of gamma hydroxybutyric on naloxone-precipitated opiate withdrawal.


Condition Intervention Phase
Opioid-Related Disorders
Drug: Gamma hydroxybutyric
Phase II

U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Double-Blind, Placebo Control
Official Title: Neurobiology of Opioid Dependence: 2

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

Primary Outcome Measures:
  • Behavioral, subjective, measures of naloxone-preci
  • Phsyiological, neuroendocrine measures of naloxone

Estimated Enrollment: 0
Study Start Date: January 1996
  Eligibility

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: NCT00000193

Locations
United States, Connecticut
VA Connecticut Healthcare System
New Haven, Connecticut, United States, 06519
Sponsors and Collaborators
Yale University
Investigators
Principal Investigator: Marc I Rosen, M.D. VA Connecticut Healthcare System
  More Information

Study ID Numbers: NIDA-00191-2, K20-00191-2
Study First Received: September 20, 1999
Last Updated: June 23, 2005
ClinicalTrials.gov Identifier: NCT00000193  
Health Authority: United States: Federal Government

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

ClinicalTrials.gov processed this record on January 15, 2009