Withdrawn
Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment I(2)
Led by University of Colorado, Denver · Updated on 2017-05-04
N/A
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Colorado, Denver
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to compare the clinical efficacy of daily vs. 3-day (MWF) buprenorphine/naloxone combination tablet administration and determine whether outcomes are improved when using a 3-day schedule in which all doses are ingested at the clinic vs. one in which take-home doses are given on intervening days.
CONDITIONS
Official Title
Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment I(2) - 2
Who Can Participate
Eligibility Criteria
You may qualify if you...
Individual must be currently dependent and meet FDA criteria for narcotic maintenance treatment. Co-morbid substance abuse or dependence disorders may also be present. Individuals must be healthy despite drug dependency.
You will not qualify if you...
Individuals with evidence of an active Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) Axis I psychiatric disorder (e.g., psychosis, manic-depressive illness, organic psychiatric disorders), significant medical illness (e.g. liver or cardiovascular disease) or pregnant female subjects are excluded from study participation.
Trial Site Locations
Total: 1 location
1
University of Colorado Health Sciences Center
Denver, Colorado, United States, 80206
Status Unknown
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
N/A
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
0
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