Clinical Trials Directory

Trials / Completed

CompletedNCT00218101

Buprenorphine as a Treatment for Individuals Dependent on Analgesic Opioids

Dose Reduction Strategies in Oral Opioid Dependence Subsequent to Pain Management: An Exploratory Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
10 (planned)
Sponsor
National Institute on Drug Abuse (NIDA) · NIH
Sex
All
Age
25 Years – 55 Years
Healthy volunteers
Accepted

Summary

Opioids used to treat chronic pain have a high abuse potential. The purpose of this study is to determine the effectiveness of buprenorphine in treating opioid dependent individuals who abuse opioids that are prescribed for chronic pain.

Detailed description

Many individuals who take opioids for chronic pain abuse the opioid medication. Buprenorphine is an opioid partial agonist that may be effective in treating individuals who abuse opiate pain medication. The purpose of this study is to compare two buprenorphine dosing regimens in order to determine which regimen is more effective in reducing opiate pain medication use and facilitating successful opioid detoxification. This study will last 27 weeks. Participants will receive a maintenance dose of 8 mg of buprenorphine for 6 weeks, followed by a dose reduction in 2 mg increments over the course of the following 20 weeks. All participants will attend weekly clinical management sessions for the duration of the study.

Conditions

Interventions

TypeNameDescription
DRUGBuprenorphine

Timeline

Start date
2004-05-01
Completion
2005-03-01
First posted
2005-09-22
Last updated
2017-01-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00218101. Inclusion in this directory is not an endorsement.