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| Sponsor: | National Institute on Drug Abuse (NIDA) |
|---|---|
| Collaborator: |
University of Vermont |
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00000231 |
Purpose
The purpose of this study is to evaluate buprenorphine and behavioral treatment with and without contingent payment on compliance with pro-social activities. In addition, we will examine whether blind naltrexone dosing is effective in indicating naltrexone consumption.
| Condition | Intervention | Phase |
|---|---|---|
|
Opioid-Related Disorders |
Drug: Buprenorphine |
Phase II |
| Study Type: | Interventional |
| Study Design: | Primary Purpose: Treatment |
| Official Title: | Buprenorphine Detoxification With Two Types of Treatment. BBD IV |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Please contact site for information.
Contacts and Locations| United States, Vermont | |
| Treatment Research Center | |
| Burlington, Vermont, United States, 05401 | |
| Principal Investigator: | Warren Bickel, Ph.D. | University of Vermont |
More Information
| ClinicalTrials.gov Identifier: | NCT00000231 History of Changes |
| Other Study ID Numbers: | NIDA-06969-13, R01-06969-13 |
| Study First Received: | September 20, 1999 |
| Last Updated: | August 16, 2005 |
| Health Authority: | United States: Federal Government |
|
Opioid-Related Disorders Substance-Related Disorders Mental Disorders Buprenorphine Analgesics, Opioid Analgesics Sensory System Agents Peripheral Nervous System Agents |
Physiological Effects of Drugs Pharmacologic Actions Central Nervous System Agents Therapeutic Uses Central Nervous System Depressants Narcotic Antagonists Narcotics |