Opioid-Related Disorders Clinical Trial
Official title:
Alternate-Day Buprenorphine Administration. Phase II
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.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 28 Years to 45 Years |
Eligibility | Please contact site for information. |
Intervention Model: Crossover Assignment, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Treatment Research Center | Burlington | Vermont |
Lead Sponsor | Collaborator |
---|---|
National Institute on Drug Abuse (NIDA) | University of Vermont |
United States,
Amass, bickel, Crean, Blake, Higgins (in press). Alternate day buprenorphine dosing as efficacious and preferred to daily dosing in opioid dependent humans. Psychopharmacology. Amass, Bickel, Crean, Blake, Higgins. (in press) Alternate day buprenorphine dosing as efficacious and preferred to daily dosing in opioid dependent humans. Psychopharmacology
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Drug use | |||
Primary | Opioid withdrawal | |||
Primary | Opioid agonist effects | |||
Primary | Dose identification | |||
Primary | Pupil diameter |
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