Opioid-Related Disorders
Conditions
Brief summary
The purpose of this study is to evaluate open buprenorphine dosing with dose choice.
Interventions
DRUGBuprenorphine
Sponsors
National Institute on Drug Abuse (NIDA)
University of Vermont
Study design
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
25 Years to 48 Years
Healthy volunteers
No
Inclusion criteria
Please contact site for information.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Drug use | — |
| Opioid withdrawal | — |
| Opioid agonist effects | — |
| Dose choice | — |
Countries
United States
Outcome results
None listed