Buprenorphine Pharmacology Related to Addiction Treatment - 21
2 other identifiers
interventional
N/A
1 country
1
Brief Summary
The purpose of this study is to examine if chronic buprenorphine administration will generate supersensitivity to opiates.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 20, 1999
CompletedFirst Posted
Study publicly available on registry
September 21, 1999
CompletedAugust 17, 2005
December 1, 2002
September 20, 1999
August 16, 2005
Conditions
Outcome Measures
Primary Outcomes (4)
Drug use
Opioid agonist effects
Opiate withdrawal
Physiological changes in: pupil diameter, blood pressure, heart rate, respiration
Interventions
Eligibility Criteria
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Sponsors & Collaborators
- National Institute on Drug Abuse (NIDA)lead
- University of Vermontcollaborator
Study Sites (1)
Treatment Research Center
Burlington, Vermont, 05401, United States
Related Publications (1)
Bickel, Amass (1995 Experimental & Clinical Psychopharmacology. 3: 477-489 Amass et al 91996) Journal of Substance Abuse Treatment. 13: 43-49 Madden et al., (1997) Experimental & Clinical Psychopharmacology. 5: 1-7. Bickel, Amass (1995) Experimental & Clinical Psychopharmacology. 3: 477-489. Amass et al., (1996) Journal of Substance Abuse Treatment. 13:43-49. Madden et al., (1997) ) Experimental & Clinical Psychopharmacology. 5:1-7.
BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Warren Bickel, Ph.D.
University of Vermont
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Purpose
- TREATMENT
- Sponsor Type
- NIH
Study Record Dates
First Submitted
September 20, 1999
First Posted
September 21, 1999
Last Updated
August 17, 2005
Record last verified: 2002-12