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| Descriptive Information Fields | |||||
| Brief Title † | Alternate Day Buprenorphine Administration, Phase XII - 17 | ||||
| Official Title † | Alternate Day Buprenorphine Administration, Phase XII | ||||
| Brief Summary | The purpose of this study is to determine if six times daily buprenorphine dose is effective in achieving 120 hour buprenorphine dosing. |
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| Detailed Description | |||||
| Study Phase | Phase II | ||||
| Study Type † | Interventional | ||||
| Study Design † | Treatment, Placebo Control, Crossover Assignment | ||||
| Primary Outcome Measure † | Drug use Opioid withdrawal Opioid agonist effects Dose choice |
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| Secondary Outcome Measure † | |||||
| Condition † | Opioid-Related Disorders | ||||
| Intervention † | Drug: Buprenorphine | ||||
| MEDLINE PMIDs | |||||
| Links | |||||
| Recruitment Information Fields | |||||
| Recruitment Status † | Completed | ||||
| Enrollment † | 0 | ||||
| Start Date † | |||||
| Completion Date | |||||
| Eligibility Criteria † | Please contact site for information. |
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| Gender | Both | ||||
| Ages | 18 Years and older | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts †† | |||||
| Location Countries † | United States | ||||
| Administrative Information Fields | |||||
| NCT ID † | NCT00000235 | ||||
| Organization ID | NIDA-06969-17 | ||||
| Secondary IDs †† | R01-06969-17 | ||||
| Study Sponsor † | National Institute on Drug Abuse (NIDA) | ||||
| Collaborators †† | University of Vermont | ||||
| Investigators † |
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| Information Provided By | National Institute on Drug Abuse (NIDA) | ||||
| Verification Date | December 2002 | ||||
| First Received Date † | September 20, 1999 | ||||
| Last Updated Date | August 16, 2005 | ||||
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