|
|
|
|
|
|
Sponsors and Collaborators: |
National Institute on Drug Abuse (NIDA) Yale University |
Information provided by: | National Institute on Drug Abuse (NIDA) |
ClinicalTrials.gov Identifier: | NCT00000193 |
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 |
Study Type: | Interventional |
Study Design: | Treatment, Double-Blind, Placebo Control |
Official Title: | Neurobiology of Opioid Dependence: 2 |
Genders Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
Please contact site for information.
United States, Connecticut | |||||
VA Connecticut Healthcare System | |||||
New Haven, Connecticut, United States, 06519 |
National Institute on Drug Abuse (NIDA) |
Yale University |
Principal Investigator: | Marc I Rosen, M.D. | VA Connecticut Healthcare System |
Study ID Numbers: | NIDA-00191-2, K20-00191-2 |
First Received: | September 20, 1999 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00000193 |
Health Authority: | United States: Federal Government |
|