Clinical Trials Directory

Trials / Completed

CompletedNCT00032955

Buprenorphine/Naloxone Versus Clonidine for Inpatient Opiate Detoxification - 1

Buprenorphine/Naloxone Versus Clonidine for Inpatient Opiate Detoxification

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
163 (planned)
Sponsor
University of California, Los Angeles · Academic / Other
Sex
All
Age
15 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess buprenorphine/naloxone versus clonidine for inpatient opiate detoxification.

Detailed description

Patients randomized to the BUP/NX arm will receive daily doses for 13 days with sublingual administration of 2 mg buprenorphine/0.5 mg naloxone tablet(s) and/or an 8 mg buprenorphine/2.0 mg naloxone tablet(s). The starting dose on day 1 is 4 mg/1 mg BUP/NX with an additional 4 mg/1 mg, if needed, escalating in a step-wise manner to 16 mg/4 mg BUP/NX on day 3 and tapering to 2 mg/ 0.5 mg BUP/NX by days 12 to 13. Patients randomized to the clonidine arm will receive oral clonidine (0.05 to 0.1 mg depending upon weight) every 4 to 6 hours for 24 hours not to exceed 0.6 mg total on day 1. On day 2, a clonidine transdermal patch will be applied (0.1 mg/day/7-day patch with number of patches adjusted by weight). Oral clonidine will continue to be given on the second day of detoxification and increased to 0.2 mg every 6 hours or 0.1 mg every 3 hours not to exceed 0.8 mg over 24 hours. Patches will be worn all 13 days of detoxification. The dose of clonidine will be adjusted according to the proposed detoxification schedule, patient's weight, tolerance, and systolic blood pressure. Patients will receive counseling according to procedures in existence at each CTP throughout the study. Self-help detoxification handbooks will be distributed to all study participants.

Conditions

Interventions

TypeNameDescription
DRUGBuprenorphine/naloxone

Timeline

Start date
2001-02-01
Primary completion
2002-08-01
Completion
2002-08-01
First posted
2002-04-08
Last updated
2017-01-12

Locations

6 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00032955. Inclusion in this directory is not an endorsement.