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Trials / Withdrawn

WithdrawnNCT00000326

Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment 1 - 1

Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment 1(1)

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of Colorado, Denver · Academic / Other
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the clinical efficacy of the buprenorphine/naloxone combination tablet for alternate-day dosing and determine whether multiples of the daily dose are necessary to maintain an effective alternate day dosing regimen.

Detailed description

Alternate-day dosing with the 8mg buprenorphine-naloxone tablet is as safe and effective as daily dosing. Outcomes are improved when the total weekly dose provided during alternate-day dosing is equal to that given during daily dosing.

Conditions

Interventions

TypeNameDescription
DRUGHeroin Dependence

Timeline

Start date
1997-04-01
Primary completion
1997-08-01
Completion
1997-08-01
First posted
1999-09-21
Last updated
2017-05-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00000326. Inclusion in this directory is not an endorsement.

Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment 1 - 1 (NCT00000326) · Clinical Trials Directory