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Buprenorphine Detoxification With Two Types of Treatment. BBD IV - 13

Primary Purpose

Opioid-Related Disorders

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Buprenorphine
Sponsored by
National Institute on Drug Abuse (NIDA)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid-Related Disorders

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Please contact site for information.

Sites / Locations

  • Treatment Research Center

Outcomes

Primary Outcome Measures

Drug use
Retention
Weeks abstinent
Weeks continuous abstinence
Overall treatment outcome
Naltrexone consumption

Secondary Outcome Measures

Full Information

First Posted
September 20, 1999
Last Updated
August 16, 2005
Sponsor
National Institute on Drug Abuse (NIDA)
Collaborators
University of Vermont
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1. Study Identification

Unique Protocol Identification Number
NCT00000231
Brief Title
Buprenorphine Detoxification With Two Types of Treatment. BBD IV - 13
Official Title
Buprenorphine Detoxification With Two Types of Treatment. BBD IV
Study Type
Interventional

2. Study Status

Record Verification Date
March 1994
Overall Recruitment Status
Completed
Study Start Date
February 1992 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute on Drug Abuse (NIDA)
Collaborators
University of Vermont

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate buprenorphine and behavioral treatment with and without contingent payment on compliance with pro-social activities. In addition, we will examine whether blind naltrexone dosing is effective in indicating naltrexone consumption.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid-Related Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Enrollment
0 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Buprenorphine
Primary Outcome Measure Information:
Title
Drug use
Title
Retention
Title
Weeks abstinent
Title
Weeks continuous abstinence
Title
Overall treatment outcome
Title
Naltrexone consumption

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Please contact site for information.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Warren Bickel, Ph.D.
Organizational Affiliation
University of Vermont
Official's Role
Principal Investigator
Facility Information:
Facility Name
Treatment Research Center
City
Burlington
State/Province
Vermont
ZIP/Postal Code
05401
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
34102902
Citation
Bunyoz KI, Tsikandylakis G, Mortensen K, Gromov K, Mohaddes M, Malchau H, Troelsen A. No difference in whole-blood metal ions between 32-mm and 36- to 44-mm femoral heads in metal-on-polyethylene total hip arthroplasty: a 2-year report from a randomised control trial. Hip Int. 2023 Mar;33(2):184-192. doi: 10.1177/11207000211022623. Epub 2021 Jun 8.
Results Reference
derived

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Buprenorphine Detoxification With Two Types of Treatment. BBD IV - 13

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