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| Sponsors and Collaborators: |
National Institute on Drug Abuse (NIDA) Yale University |
|---|---|
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00000196 |
Purpose
The purpose of this study is to determine the effect of acute naltrexone pretreatment on the response to yohimbine in healthy volunteers.
| Condition | Intervention | Phase |
|---|---|---|
|
Opioid-Related Disorders |
Drug: Naltrexone |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Double-Blind, Placebo Control |
| Official Title: | Neurobiology of Opioid Dependence: 5 |
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Please contact site for information.
Contacts and Locations| United States, Connecticut | |
| VA Connecticut Healthcare System | |
| New Haven, Connecticut, United States, 06519 | |
| Principal Investigator: | Marc I Rosen, M.D. | VA Connecticut Healthcare System |
More Information
| Study ID Numbers: | NIDA-00191-5, K20-00191-5 |
| Study First Received: | September 20, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00000196 History of Changes |
| Health Authority: | United States: Federal Government |
|
Mental Disorders Narcotic Antagonists Naltrexone Substance-Related Disorders |
Disorders of Environmental Origin Narcotics Peripheral Nervous System Agents Opioid-Related Disorders |
|
Sensory System Agents Mental Disorders Therapeutic Uses Physiological Effects of Drugs Narcotic Antagonists Naltrexone |
Substance-Related Disorders Disorders of Environmental Origin Peripheral Nervous System Agents Opioid-Related Disorders Central Nervous System Agents Pharmacologic Actions |