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Sponsored by: |
National Institute on Drug Abuse (NIDA) |
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Information provided by: | National Institute on Drug Abuse (NIDA) |
ClinicalTrials.gov Identifier: | NCT00000202 |
The purpose of this study is to evaluate the efficacy of buprenorphine and desipramine in treatment of opiate and cocaine dependence.
Condition | Intervention | Phase |
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Opioid-Related Disorders |
Drug: Buprenorphine |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Uncontrolled |
Official Title: | Buprenorphine Maintenance for Opioid Addicts |
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Please contact site for information.
United States, Connecticut | |
VA Connecticut Healthcare System | |
New Haven, Connecticut, United States, 06519 |
Principal Investigator: | Thomas R Kosten, M.D. | VA Connecticut Healthcare System |
Study ID Numbers: | NIDA-05626-1, R01-05626-1 |
Study First Received: | September 20, 1999 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00000202 |
Health Authority: | United States: Federal Government |
Buprenorphine Mental Disorders Substance-Related Disorders Disorders of Environmental Origin Opioid-Related Disorders |
Sensory System Agents Therapeutic Uses Narcotic Antagonists Physiological Effects of Drugs Central Nervous System Depressants Narcotics |
Peripheral Nervous System Agents Analgesics Central Nervous System Agents Pharmacologic Actions Analgesics, Opioid |