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| Sponsor: | National Institute on Drug Abuse (NIDA) |
|---|---|
| Collaborator: |
Yale University |
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00000319 |
Purpose
The purpose of this study is to evaluate the efficacy of treating opioid-dependent individuals with buprenorphine on a thrice-weekly schedule compared to daily dosing.
| Condition | Intervention | Phase |
|---|---|---|
|
Opioid-Related Disorders Substance-Related Disorders |
Drug: Buprenorphine |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment |
| Official Title: | Buprenorphine Maintenance Dose Schedule and Treatment Setting |
Eligibility| Ages Eligible for Study: | 21 Years to 55 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Please contact site for information.
Contacts and Locations| United States, Connecticut | |
| APT Residential Services Division | |
| New Haven, Connecticut, United States, 06519 | |
| Principal Investigator: | Richard Schottenfeld, M.D. | Yale University |
More Information
| Study ID Numbers: | NIDA-09803-2, R01-09803-2 |
| Study First Received: | September 20, 1999 |
| Last Updated: | August 16, 2005 |
| ClinicalTrials.gov Identifier: | NCT00000319 History of Changes |
| Health Authority: | United States: Federal Government |
|
Disease Narcotic Antagonists Physiological Effects of Drugs Central Nervous System Depressants Disorders of Environmental Origin Narcotics Opioid-Related Disorders Pharmacologic Actions Buprenorphine |
Pathologic Processes Mental Disorders Sensory System Agents Therapeutic Uses Substance-Related Disorders Analgesics Peripheral Nervous System Agents Central Nervous System Agents Analgesics, Opioid |