Alternate-Day Buprenorphine Administration. Phase I - 3
Completed · Phase 1
Conditions studied: Opioid-Related Disorders
In brief
The purpose of this study is to determine if two times a subject's daily maintenance dose will hold for 48 hours without changes in agonist and antagonist effects.
Key facts
- Study ID
- NCT00000221
- Run by
- National Institute on Drug Abuse (NIDA)
- People needed
- 0
- Starts
- 1992-04-01
- Last updated by the study team
- 2005-06-24
Who can join
Age: 28 and older, up to 45. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Treatment Research Center — Burlington, Vermont, United States
Full record on ClinicalTrials.gov
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