Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DRUG | Heroin 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.