|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | National Institute on Drug Abuse (NIDA) |
|---|---|
| Collaborator: |
University of Vermont |
| Information provided by: | National Institute on Drug Abuse (NIDA) |
| ClinicalTrials.gov Identifier: | NCT00000227 |
Purpose
The purpose of this study is to evaluate open buprenorphine dosing with dose choice.
| Condition | Intervention | Phase |
|---|---|---|
|
Opioid-Related Disorders |
Drug: Buprenorphine |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Placebo Control, Crossover Assignment |
| Official Title: | Alternate-Day Buprenorphine Administration. Phase VIII |
Eligibility| Ages Eligible for Study: | 25 Years to 48 Years |
| 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
| Study ID Numbers: | NIDA-06969-9, R01-06969-9 |
| Study First Received: | September 20, 1999 |
| Last Updated: | August 16, 2005 |
| ClinicalTrials.gov Identifier: | NCT00000227 History of Changes |
| Health Authority: | United States: Federal Government |
|
Narcotic Antagonists Physiological Effects of Drugs Central Nervous System Depressants Disorders of Environmental Origin Narcotics Opioid-Related Disorders Pharmacologic Actions Buprenorphine |
Mental Disorders Sensory System Agents Therapeutic Uses Substance-Related Disorders Analgesics Peripheral Nervous System Agents Central Nervous System Agents Analgesics, Opioid |