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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: | NCT00000235 |
Purpose
The purpose of this study is to determine if six times daily buprenorphine dose is effective in achieving 120 hour buprenorphine dosing.
| Condition | Intervention | Phase |
|---|---|---|
|
Opioid-Related Disorders |
Drug: Buprenorphine |
Phase II |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Crossover Assignment Primary Purpose: Treatment |
| Official Title: | Alternate Day Buprenorphine Administration, Phase XII |
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: | NCT00000235 History of Changes |
| Other Study ID Numbers: | NIDA-06969-17, R01-06969-17 |
| 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 |